Validation pour Ingenuity370

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Ingenuity370

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Phrase 2 - PMID ?

Mutant SP NODE gene ( homozygous null mutation ) in SP exhibiting familial hypercholesterolemia increases localization of NODE protein in NODE fraction .

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

Commentaires :

Analyse 0

                                                                         +-------------------------------------COMP:V-N(in)------------------------------------+              
                                                                         +----------------------OBJ:V-N----------------------+                                 |              
                   +-------------APPOS-------------+                     |         +--------------MOD_ATT:N-ADJ--------------+                                 |              
                   |                +-MOD_ATT:N-ADJ+                     |         |              +--------MOD_ATT:N-N-------+-----COMP:N-N(of)----+           |              
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+           |              
           |       |                |       |      |            |        |         |              |              |           |             |       |           |              
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
COMP:V-N(in) (exhibit,__NODE__)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
COMP:N-N(of) (localization,protein)
MOD_ATT:N-ADJ (protein,__NODE__)

Analyse 1

                                                                         +----------------------OBJ:V-N----------------------+                                                
                   +-------------APPOS-------------+                     |         +--------------MOD_ATT:N-ADJ--------------+                                                
                   |                +-MOD_ATT:N-ADJ+                     |         |              +--------MOD_ATT:N-N-------+-----COMP:N-N(of)----+                          
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+                          
           |       |                |       |      |            |        |         |              |              |           |             |       |                          
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
COMP:N-N(of) (localization,protein)
MOD_ATT:N-ADJ (protein,__NODE__)

Analyse 2

                                                                +-----------------------------------COMP:N-N(of)-----------------------------------+                          
                                                                |        +----------------------OBJ:V-N----------------------+                     |                          
                   +-------------APPOS-------------+            |        |         +--------------MOD_ATT:N-ADJ--------------+                     |                          
                   |                +-MOD_ATT:N-ADJ+            |        |         |              +--------MOD_ATT:N-N-------+                     |                          
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+                          
           |       |                |       |      |            |        |         |              |              |           |             |       |                          
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
COMP:N-N(of) (__SP__,protein)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
MOD_ATT:N-ADJ (protein,__NODE__)

Analyse 3

                                                                         +----------------------OBJ:V-N----------------------+                                                
                   +-------------APPOS-------------+                     |         +--------------MOD_ATT:N-ADJ--------------+                                                
                   |                +-MOD_ATT:N-ADJ+                     |         |              +--------MOD_ATT:N-N-------+-----COMP:N-N(of)----+                          
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+COMP:N-N(in+              
           |       |                |       |      |            |        |         |              |              |           |             |       |           |              
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
COMP:N-N(of) (localization,protein)
MOD_ATT:N-ADJ (protein,__NODE__)
COMP:N-N(in) (protein,__NODE__)

Analyse 4

                                                                         +----------------------OBJ:V-N----------------------+                                                
                   +-------------APPOS-------------+                     |         +--------------MOD_ATT:N-ADJ--------------+-----------COMP:N-N(in)----------+              
                   |                +-MOD_ATT:N-ADJ+                     |         |              +--------MOD_ATT:N-N-------+-----COMP:N-N(of)----+           |              
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+           |              
           |       |                |       |      |            |        |         |              |              |           |             |       |           |              
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
COMP:N-N(of) (localization,protein)
COMP:N-N(in) (localization,__NODE__)
MOD_ATT:N-ADJ (protein,__NODE__)

Analyse 5

                                                                +-----------------------------------COMP:N-N(of)-----------------------------------+                          
                                                                |        +----------------------OBJ:V-N----------------------+                     |                          
                   +-------------APPOS-------------+            |        |         +--------------MOD_ATT:N-ADJ--------------+                     |                          
                   |                +-MOD_ATT:N-ADJ+            |        |         |              +--------MOD_ATT:N-N-------+                     |                          
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+COMP:N-N(in+              
           |       |                |       |      |            |        |         |              |              |           |             |       |           |              
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
COMP:N-N(of) (__SP__,protein)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
MOD_ATT:N-ADJ (protein,__NODE__)
COMP:N-N(in) (protein,__NODE__)

Analyse 6

                                                                +-----------------------------------------COMP:N-N(in)-----------------------------------------+              
                                                                |        +----------------------OBJ:V-N----------------------+                                 |              
                   +-------------APPOS-------------+            |        |         +--------------MOD_ATT:N-ADJ--------------+                                 |              
                   |                +-MOD_ATT:N-ADJ+            |        |         |              +--------MOD_ATT:N-N-------+-----COMP:N-N(of)----+           |              
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+           |              
           |       |                |       |      |            |        |         |              |              |           |             |       |           |              
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
COMP:N-N(in) (__SP__,__NODE__)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
COMP:N-N(of) (localization,protein)
MOD_ATT:N-ADJ (protein,__NODE__)

Analyse 7

                                                                +-----------------------------------------COMP:N-N(in)-----------------------------------------+              
                                                                +-----------------------------------COMP:N-N(of)-----------------------------------+           |              
                                                                |        +----------------------OBJ:V-N----------------------+                     |           |              
                   +-------------APPOS-------------+            |        |         +--------------MOD_ATT:N-ADJ--------------+                     |           |              
                   |                +-MOD_ATT:N-ADJ+            |        |         |              +--------MOD_ATT:N-N-------+                     |           |              
           +OBJ:V-N+                |       +MOD_AT+            +SUBJ:V-N+         |              |              +MOD_ATT:N-N+             +MOD_ATT+           |              
           |       |                |       |      |            |        |         |              |              |           |             |       |           |              
 Mutant __SP__ __NODE__ gene ( homozygous null mutation ) in __SP__ exhibiting familial hypercholesterolemia increases localization of __NODE__ protein in __NODE__ fraction .
OBJ:V-N (__SP__,__NODE__)
APPOS (__NODE__,mutation)
MOD_ATT:N-ADJ (mutation,homozygous)
MOD_ATT:N-ADJ (mutation,null)
COMP:N-N(of) (__SP__,protein)
COMP:N-N(in) (__SP__,__NODE__)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,localization)
MOD_ATT:N-ADJ (localization,familial)
MOD_ATT:N-N (localization,hypercholesterolemia)
MOD_ATT:N-N (localization,increase)
MOD_ATT:N-ADJ (protein,__NODE__)