Validation pour Ingenuity410

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Ingenuity410

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Phrase 58 - PMID ?

Premature coronary artery disease in humans is associated with mutant SP NODE protein ( unspecified heterozygous gene mutation ) in SP exhibiting familial hypercholesterolemia .

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

Commentaires :

Analyse 0

                                                     +-------------------------------------COMP:V_PASS-N(in)------------------------------------+                                             
                                                     +---------COMP:V_PASS-N(with)--------+------------------APPOS-----------------+            |                                             
     +------MOD_ATT:N-ADJ-----+                      |             +-----MOD_ATT:N-ADJ----+           +--------MOD_ATT:N-ADJ-------+            |                                             
     |         +--MOD_ATT:N-N-+-----SUBJ:V_PASS-N----+             |      +-MOD_ATT:N-ADJ-+           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     |         |       +MOD_AT+COMP:N-N(i+           |             |      |       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |         |       |      |          |           |             |      |       |       |           |            |        |      |            |        |         |              |           
 Premature coronary artery disease in humans is associated with mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-ADJ (disease,premature)
MOD_ATT:N-N (disease,coronary)
MOD_ATT:N-N (disease,artery)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,protein)
COMP:V_PASS-N(in) (associate,__SP__)
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)--------+------------------APPOS-----------------+            |                                             
     +------MOD_ATT:N-ADJ-----+                      |             +-----MOD_ATT:N-ADJ----+           +--------MOD_ATT:N-ADJ-------+            |                                             
     |         +-MOD_ATT:N-ADJ+-----SUBJ:V_PASS-N----+             |      +-MOD_ATT:N-ADJ-+           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     |         |       +MOD_AT+COMP:N-N(i+           |             |      |       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |         |       |      |          |           |             |      |       |       |           |            |        |      |            |        |         |              |           
 Premature coronary artery disease in humans is associated with mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-ADJ (disease,premature)
MOD_ATT:N-ADJ (disease,coronary)
MOD_ATT:N-N (disease,artery)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,protein)
COMP:V_PASS-N(in) (associate,__SP__)
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)------------------------------------+                                             
                                                     |                                    +------------------APPOS-----------------+            |                                             
     +------MOD_ATT:N-ADJ-----+                      |       +-----------OBJ:V-N----------+           +--------MOD_ATT:N-ADJ-------+            |                                             
     |         +--MOD_ATT:N-N-+-----SUBJ:V_PASS-N----+-COMP:V_PASS-N(with)+               |           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     |         |       +MOD_AT+COMP:N-N(i+           |       |     +MOD_AT+       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |         |       |      |          |           |       |     |      |       |       |           |            |        |      |            |        |         |              |           
 Premature coronary artery disease in humans is associated with mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-ADJ (disease,premature)
MOD_ATT:N-N (disease,coronary)
MOD_ATT:N-N (disease,artery)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
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 3

                                                     +-------------------------------------COMP:V_PASS-N(in)------------------------------------+                                             
                                                     |                                    +------------------APPOS-----------------+            |                                             
     +------MOD_ATT:N-ADJ-----+                      |       +-----------OBJ:V-N----------+           +--------MOD_ATT:N-ADJ-------+            |                                             
     |         +-MOD_ATT:N-ADJ+-----SUBJ:V_PASS-N----+-COMP:V_PASS-N(with)+               |           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     |         |       +MOD_AT+COMP:N-N(i+           |       |     +MOD_AT+       +MOD_ATT+           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |         |       |      |          |           |       |     |      |       |       |           |            |        |      |            |        |         |              |           
 Premature coronary artery disease in humans is associated with mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-ADJ (disease,premature)
MOD_ATT:N-ADJ (disease,coronary)
MOD_ATT:N-N (disease,artery)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
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)----+       +------------------APPOS-----------------+            |                                             
     +------MOD_ATT:N-ADJ-----+                      |       +-----------OBJ:V-N----------+           +--------MOD_ATT:N-ADJ-------+            |                                             
     |         +--MOD_ATT:N-N-+-----SUBJ:V_PASS-N----+       |     +-MOD_ATT:N-ADJ+       |           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     |         |       +MOD_AT+COMP:N-N(i+           |       |     |      +MOD_ATT+       |           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |         |       |      |          |           |       |     |      |       |       |           |            |        |      |            |        |         |              |           
 Premature coronary artery disease in humans is associated with mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-ADJ (disease,premature)
MOD_ATT:N-N (disease,coronary)
MOD_ATT:N-N (disease,artery)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
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)

Analyse 5

                                                     +-------------------------------------COMP:V_PASS-N(in)------------------------------------+                                             
                                                     +-----COMP:V_PASS-N(with)----+       +------------------APPOS-----------------+            |                                             
     +------MOD_ATT:N-ADJ-----+                      |       +-----------OBJ:V-N----------+           +--------MOD_ATT:N-ADJ-------+            |                                             
     |         +-MOD_ATT:N-ADJ+-----SUBJ:V_PASS-N----+       |     +-MOD_ATT:N-ADJ+       |           |            +-MOD_ATT:N-ADJ-+            |        +---------OBJ:V-N--------+           
     |         |       +MOD_AT+COMP:N-N(i+           |       |     |      +MOD_ATT+       |           |            |        +MOD_AT+            +SUBJ:V-N+         +-MOD_ATT:N-ADJ+           
     |         |       |      |          |           |       |     |      |       |       |           |            |        |      |            |        |         |              |           
 Premature coronary artery disease in humans is associated with mutant __SP__ __NODE__ protein ( unspecified heterozygous gene mutation ) in __SP__ exhibiting familial hypercholesterolemia .
MOD_ATT:N-ADJ (disease,premature)
MOD_ATT:N-ADJ (disease,coronary)
MOD_ATT:N-N (disease,artery)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,protein)
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)