Validation pour Ingenuity160

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Ingenuity160

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Phrase 19 - PMID ?

Familial hypercholesterolemia in humans is associated with mutant SP NODE gene ( insertion from a DNA fragment containing a exon 3 6 from SP NODE gene ) .

Non annotée
Je ne sais pas
Je n'ai pas trouvé d'analyse satisfaisante

Commentaires :

Analyse 0

                                                 +-----COMP:V_PASS-N(with)----+                                                        +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+                   |    +-----SUBJ:V-N----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+    +COMP:N-N(+       |            
     |              |                |           |             |      |       |               |             |      |         |         |    |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (6,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,6)

Analyse 1

                                                 +-----COMP:V_PASS-N(with)----+                                                        +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+                   |  +------SUBJ:V-N-----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  +COMP:N-N(fr+       |            
     |              |                |           |             |      |       |               |             |      |         |         |  |           |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (3,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 2

                                                                                                                                       +--------OBJ:V-N-------+            
                                                 +-----COMP:V_PASS-N(with)----+                                                        |  +------SUBJ:V-N-----+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+                   |  +--OBJ:V-N--+       |            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  | +-SUBJ:V-N+       |            
     |              |                |           |             |      |       |               |             |      |         |         |  | |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
OBJ:V-N (__SP__,3)
SUBJ:V-N (__SP__,6)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 3

                                                 +-----COMP:V_PASS-N(with)----+               +-----------SUBJ:V-N-----------+         +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+         |         |    +-----SUBJ:V-N----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+         +-OBJ:V-N-+    +COMP:N-N(+       |            
     |              |                |           |             |      |       |               |             |      |         |         |    |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,insertion)
OBJ:V-N (contain,exon)
COMP:N-N(from) (6,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,6)

Analyse 4

                                                 +-----COMP:V_PASS-N(with)----+               +-----------SUBJ:V-N-----------+         +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+         |         |  +------SUBJ:V-N-----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+         +-OBJ:V-N-+  +COMP:N-N(fr+       |            
     |              |                |           |             |      |       |               |             |      |         |         |  |           |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,insertion)
OBJ:V-N (contain,exon)
COMP:N-N(from) (3,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 5

                                                 +-----COMP:V_PASS-N(with)----+                                    +------------------OBJ:V-N-----------------+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+                        +-----SUBJ:V-N----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+    +COMP:N-N(+       |            
     |              |                |           |             |      |       |               |             |      |         |         |    |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (6,__SP__)
OBJ:V-N (__NODE__,fragment)
SUBJ:V-N (__NODE__,6)

Analyse 6

                                                 +-----COMP:V_PASS-N(with)----+                                    +------------------OBJ:V-N-----------------+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+                      +------SUBJ:V-N-----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  +COMP:N-N(fr+       |            
     |              |                |           |             |      |       |               |             |      |         |         |  |           |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (3,__SP__)
OBJ:V-N (__NODE__,fragment)
SUBJ:V-N (__NODE__,3)

Analyse 7

                                                                                                                                       +--------OBJ:V-N-------+            
                                                 +-----COMP:V_PASS-N(with)----+               +-----------SUBJ:V-N-----------+         |  +------SUBJ:V-N-----+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+         |         |  +--OBJ:V-N--+       |            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+         +-OBJ:V-N-+  | +-SUBJ:V-N+       |            
     |              |                |           |             |      |       |               |             |      |         |         |  | |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,insertion)
OBJ:V-N (contain,exon)
OBJ:V-N (__SP__,3)
SUBJ:V-N (__SP__,6)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 8

                                                                                                                   +------------------OBJ:V-N-----------------+            
                                                 +-----COMP:V_PASS-N(with)----+                                    |                      +------SUBJ:V-N-----+            
                    +--------SUBJ:V_PASS-N-------+             +-MOD_ATT:N-ADJ+               +---COMP:N-N(from)---+                      +--OBJ:V-N--+       |            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |             |      +MOD_ATT+-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  | +-SUBJ:V-N+       |            
     |              |                |           |             |      |       |               |             |      |         |         |  | |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
OBJ:V-N (__SP__,3)
SUBJ:V-N (__SP__,6)
OBJ:V-N (__NODE__,fragment)
SUBJ:V-N (__NODE__,3)

Analyse 9

                                                 +-COMP:V_PASS-N(with)+                                                                +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+                   |    +-----SUBJ:V-N----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+    +COMP:N-N(+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |    |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (6,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,6)

Analyse 10

                                                 +-COMP:V_PASS-N(with)+                                                                +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+                   |  +------SUBJ:V-N-----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  +COMP:N-N(fr+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |  |           |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (3,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 11

                                                                                                                                       +--------OBJ:V-N-------+            
                                                 +-COMP:V_PASS-N(with)+                                                                |  +------SUBJ:V-N-----+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+                   |  +--OBJ:V-N--+       |            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  | +-SUBJ:V-N+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |  | |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
OBJ:V-N (__SP__,3)
SUBJ:V-N (__SP__,6)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 12

                                                 +-COMP:V_PASS-N(with)+                       +-----------SUBJ:V-N-----------+         +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+         |         |    +-----SUBJ:V-N----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+         +-OBJ:V-N-+    +COMP:N-N(+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |    |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,insertion)
OBJ:V-N (contain,exon)
COMP:N-N(from) (6,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,6)

Analyse 13

                                                 +-COMP:V_PASS-N(with)+                       +-----------SUBJ:V-N-----------+         +--------OBJ:V-N-------+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+         |         |  +------SUBJ:V-N-----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+         +-OBJ:V-N-+  +COMP:N-N(fr+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |  |           |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,insertion)
OBJ:V-N (contain,exon)
COMP:N-N(from) (3,__SP__)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 14

                                                 +-COMP:V_PASS-N(with)+                                            +------------------OBJ:V-N-----------------+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+                        +-----SUBJ:V-N----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+    +COMP:N-N(+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |    |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (6,__SP__)
OBJ:V-N (__NODE__,fragment)
SUBJ:V-N (__NODE__,6)

Analyse 15

                                                 +-COMP:V_PASS-N(with)+                                            +------------------OBJ:V-N-----------------+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+                      +------SUBJ:V-N-----+            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  +COMP:N-N(fr+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |  |           |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
COMP:N-N(from) (3,__SP__)
OBJ:V-N (__NODE__,fragment)
SUBJ:V-N (__NODE__,3)

Analyse 16

                                                                                                                                       +--------OBJ:V-N-------+            
                                                 +-COMP:V_PASS-N(with)+                       +-----------SUBJ:V-N-----------+         |  +------SUBJ:V-N-----+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+         |         |  +--OBJ:V-N--+       |            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+         +-OBJ:V-N-+  | +-SUBJ:V-N+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |  | |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,insertion)
OBJ:V-N (contain,exon)
OBJ:V-N (__SP__,3)
SUBJ:V-N (__SP__,6)
OBJ:V-N (__NODE__,exon)
SUBJ:V-N (__NODE__,3)

Analyse 17

                                                                                                                   +------------------OBJ:V-N-----------------+            
                                                 +-COMP:V_PASS-N(with)+                                            |                      +------SUBJ:V-N-----+            
                    +--------SUBJ:V_PASS-N-------+       +-------OBJ:V-N------+               +---COMP:N-N(from)---+                      +--OBJ:V-N--+       |            
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |     +MOD_AT+       +-----APPOS-----+             +MOD_AT+-SUBJ:V-N+-OBJ:V-N-+  | +-SUBJ:V-N+       |            
     |              |                |           |       |     |      |       |               |             |      |         |         |  | |         |       |            
 Familial hypercholesterolemia in humans is associated with mutant __SP__ __NODE__ gene ( insertion from a DNA fragment containing a exon 3 6 from __SP__ __NODE__ gene ) .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,insertion)
COMP:N-N(from) (insertion,fragment)
MOD_ATT:N-N (fragment,DNA)
SUBJ:V-N (contain,fragment)
OBJ:V-N (contain,exon)
OBJ:V-N (__SP__,3)
SUBJ:V-N (__SP__,6)
OBJ:V-N (__NODE__,fragment)
SUBJ:V-N (__NODE__,3)