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Phrase 44 - PMID ?

Familial hypercholesterolemia in humans is associated with nonsense mutation mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .


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


Commentaires :
Analyse 0 
                                                 +----------------------------------------------COMP:V_PASS-N(in)---------------------------------------------+                                             
                                                 |       +--------------------OBJ:V-N-------------------+------------------APPOS-----------------+            |                                             
                                                 |       |                       +-----MOD_ATT:N-ADJ----+           +--------MOD_ATT:N-ADJ-------+            |                                             
                    +--------SUBJ:V_PASS-N-------+--COMP:V_PASS-N(with)--+       |      +-MOD_ATT:N-ADJ-+           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |      +MOD_ATT:+       |      |       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |              |                |           |       |      |        |       |      |       |       |           |            |        |      |            |        |         |              |           
 Familial hypercholesterolemia in humans is associated with nonsense mutation mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,mutation)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
MOD_ATT:N-N (mutation,nonsense)
MOD_ATT:N-ADJ (protein,mutant)
MOD_ATT:N-ADJ (protein,__SP__)
MOD_ATT:N-ADJ (protein,__NODE__)
APPOS (protein,mutation)
MOD_ATT:N-ADJ (mutation,unspecified)
MOD_ATT:N-ADJ (mutation,heterozygous)
MOD_ATT:N-N (mutation,gene)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,hypercholesterolemia)
MOD_ATT:N-ADJ (hypercholesterolemia,familial)
Analyse 1 
                                                 +----------------------------------------------COMP:V_PASS-N(in)---------------------------------------------+                                             
                                                 +------------------COMP:V_PASS-N(with)-----------------+                                                     |                                             
                                                 |              +--------------MOD_ATT:N-N--------------+                                                     |                                             
                                                 |              |        +----------MOD_ATT:N-N---------+------------------APPOS-----------------+            |                                             
                                                 |              |        |       +-----MOD_ATT:N-ADJ----+           +--------MOD_ATT:N-ADJ-------+            |                                             
                    +--------SUBJ:V_PASS-N-------+              |        |       |      +-MOD_ATT:N-ADJ-+           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |              |        |       |      |       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |              |                |           |              |        |       |      |       |       |           |            |        |      |            |        |         |              |           
 Familial hypercholesterolemia in humans is associated with nonsense mutation mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,protein)
COMP:V_PASS-N(in) (associate,__SP__)
MOD_ATT:N-N (protein,nonsense)
MOD_ATT:N-N (protein,mutation)
MOD_ATT:N-ADJ (protein,mutant)
MOD_ATT:N-ADJ (protein,__SP__)
MOD_ATT:N-ADJ (protein,__NODE__)
APPOS (protein,mutation)
MOD_ATT:N-ADJ (mutation,unspecified)
MOD_ATT:N-ADJ (mutation,heterozygous)
MOD_ATT:N-N (mutation,gene)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,hypercholesterolemia)
MOD_ATT:N-ADJ (hypercholesterolemia,familial)
Analyse 2 
                                                 +----------------------------------------------COMP:V_PASS-N(in)---------------------------------------------+                                             
                                                 |       +--------------------OBJ:V-N-------------------+                                                     |                                             
                                                 |       |               +----------MOD_ATT:N-N---------+------------------APPOS-----------------+            |                                             
                                                 |       |               |       +-----MOD_ATT:N-ADJ----+           +--------MOD_ATT:N-ADJ-------+            |                                             
                    +--------SUBJ:V_PASS-N-------+       |               |       |      +-MOD_ATT:N-ADJ-+           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           +COMP:V_PASS-N(+        |       |      |       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |              |                |           |       |      |        |       |      |       |       |           |            |        |      |            |        |         |              |           
 Familial hypercholesterolemia in humans is associated with nonsense mutation mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-N (hypercholesterolemia,familial)
COMP:N-N(in) (hypercholesterolemia,human)
SUBJ:V_PASS-N (associate,hypercholesterolemia)
COMP:V_PASS-N(with) (associate,nonsense)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
MOD_ATT:N-N (protein,mutation)
MOD_ATT:N-ADJ (protein,mutant)
MOD_ATT:N-ADJ (protein,__SP__)
MOD_ATT:N-ADJ (protein,__NODE__)
APPOS (protein,mutation)
MOD_ATT:N-ADJ (mutation,unspecified)
MOD_ATT:N-ADJ (mutation,heterozygous)
MOD_ATT:N-N (mutation,gene)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,hypercholesterolemia)
MOD_ATT:N-ADJ (hypercholesterolemia,familial)
Analyse 3 
                                                 +----------------------------------------------COMP:V_PASS-N(in)---------------------------------------------+                                             
                                                 |       +--------------------OBJ:V-N-------------------+                                                     |                                             
                                                 +----------COMP:V_PASS-N(with)---------+               +------------------APPOS-----------------+            |                                             
                                                 |       |      +------MOD_ATT:N-N------+               |           +--------MOD_ATT:N-ADJ-------+            |                                             
                    +--------SUBJ:V_PASS-N-------+       |      |        +--MOD_ATT:N-N-+               |           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |      |        |       +MOD_AT+       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |              |                |           |       |      |        |       |      |       |       |           |            |        |      |            |        |         |              |           
 Familial hypercholesterolemia in humans is associated with nonsense mutation mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
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__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
MOD_ATT:N-N (__SP__,nonsense)
MOD_ATT:N-N (__SP__,mutation)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (protein,__NODE__)
APPOS (protein,mutation)
MOD_ATT:N-ADJ (mutation,unspecified)
MOD_ATT:N-ADJ (mutation,heterozygous)
MOD_ATT:N-N (mutation,gene)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,hypercholesterolemia)
MOD_ATT:N-ADJ (hypercholesterolemia,familial)
Analyse 4 
                                                 +----------------------------------------------COMP:V_PASS-N(in)---------------------------------------------+                                             
                                                 +--------------COMP:V_PASS-N(with)-------------+                                                             |                                             
                                                 |       +--------------------OBJ:V-N-------------------+                                                     |                                             
                                                 |       |      +----------MOD_ATT:N-N----------+       +------------------APPOS-----------------+            |                                             
                                                 |       |      |        +------MOD_ATT:N-N-----+       |           +--------MOD_ATT:N-ADJ-------+            |                                             
                    +--------SUBJ:V_PASS-N-------+       |      |        |       +-MOD_ATT:N-ADJ+       |           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     +--MOD_ATT:N-N-+--COMP:N-N(in)--+           |       |      |        |       |      +MOD_ATT+       |           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |              |                |           |       |      |        |       |      |       |       |           |            |        |      |            |        |         |              |           
 Familial hypercholesterolemia in humans is associated with nonsense mutation mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
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__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
MOD_ATT:N-N (__NODE__,nonsense)
MOD_ATT:N-N (__NODE__,mutation)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (protein,mutation)
MOD_ATT:N-ADJ (mutation,unspecified)
MOD_ATT:N-ADJ (mutation,heterozygous)
MOD_ATT:N-N (mutation,gene)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,hypercholesterolemia)
MOD_ATT:N-ADJ (hypercholesterolemia,familial)