vers la météo de la validation par utilisateur

Ingenuity392

precedent - 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 - suivant

Phrase 2 - PMID ?

__NODE__ palmitoyltransferase type I deficiency in humans is associated with mutant __SP__ __NODE__ gene ( C1069T ) in __SP__ exhibiting __NODE__ palmitoyltransferase type I deficiency .


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


Commentaires :
Analyse 0 
                                                       +-----------------------------------------------------SUBJ:V-N-----------------------------------------------------+                
     +------------------MOD_ATT:N-ADJ------------------+           +-------------------COMP:V_PASS-N(in)-------------------+                                              |                
     |              +------------MOD_ATT:N-N-----------+           +-----COMP:V_PASS-N(with)----+                          |                                              |                
     |              |            +-----MOD_ATT:N-N-----+           |             +-MOD_ATT:N-ADJ+                          |        +---------OBJ:V-N--------+            |                
     |              |            |         +MOD_ATT:N-N+SUBJ:V_PASS+             |      +MOD_ATT+-----APPOS----+           +SUBJ:V-N+         +-MOD_ATT:N-ADJ+            |                
     |              |            |         |           |           |             |      |       |              |           |        |         |              |            |                
 __NODE__ palmitoyltransferase type I deficiency in humans is associated with mutant __SP__ __NODE__ gene ( C1069T ) in __SP__ exhibiting __NODE__ palmitoyltransferase type I deficiency .
MOD_ATT:N-ADJ (human,__NODE__)
MOD_ATT:N-N (human,palmitoyltransferase)
MOD_ATT:N-N (human,type)
MOD_ATT:N-N (human,deficiency)
SUBJ:V_PASS-N (associate,human)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(in) (associate,__SP__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,C1069T)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,palmitoyltransferase)
MOD_ATT:N-ADJ (palmitoyltransferase,__NODE__)
SUBJ:V-N (type,human)
Analyse 1 
     +------------------MOD_ATT:N-ADJ------------------+-----------------------------------------------------SUBJ:V-N-----------------------------------------------------+                
     |              +------------MOD_ATT:N-N-----------+           +-----COMP:V_PASS-N(with)----+                                                                         |                
     |              |            +-----MOD_ATT:N-N-----+           |             +-MOD_ATT:N-ADJ+                                   +---------OBJ:V-N--------+            |                
     |              |            |         +MOD_ATT:N-N+SUBJ:V_PASS+             |      +MOD_ATT+-----APPOS----+           +SUBJ:V-N+         +-MOD_ATT:N-ADJ+            |                
     |              |            |         |           |           |             |      |       |              |           |        |         |              |            |                
 __NODE__ palmitoyltransferase type I deficiency in humans is associated with mutant __SP__ __NODE__ gene ( C1069T ) in __SP__ exhibiting __NODE__ palmitoyltransferase type I deficiency .
MOD_ATT:N-ADJ (human,__NODE__)
MOD_ATT:N-N (human,palmitoyltransferase)
MOD_ATT:N-N (human,type)
MOD_ATT:N-N (human,deficiency)
SUBJ:V_PASS-N (associate,human)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (__NODE__,C1069T)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,palmitoyltransferase)
MOD_ATT:N-ADJ (palmitoyltransferase,__NODE__)
SUBJ:V-N (type,human)
Analyse 2 
                                                       +-----------------------------------------------------SUBJ:V-N-----------------------------------------------------+                
     +------------------MOD_ATT:N-ADJ------------------+           +-------------------COMP:V_PASS-N(in)-------------------+                                              |                
     |              +------------MOD_ATT:N-N-----------+           +-COMP:V_PASS-N(with)+                                  |                                              |                
     |              |            +-----MOD_ATT:N-N-----+           |       +-------OBJ:V-N------+                          |        +---------OBJ:V-N--------+            |                
     |              |            |         +MOD_ATT:N-N+SUBJ:V_PASS+       |     +MOD_AT+       +-----APPOS----+           +SUBJ:V-N+         +-MOD_ATT:N-ADJ+            |                
     |              |            |         |           |           |       |     |      |       |              |           |        |         |              |            |                
 __NODE__ palmitoyltransferase type I deficiency in humans is associated with mutant __SP__ __NODE__ gene ( C1069T ) in __SP__ exhibiting __NODE__ palmitoyltransferase type I deficiency .
MOD_ATT:N-ADJ (human,__NODE__)
MOD_ATT:N-N (human,palmitoyltransferase)
MOD_ATT:N-N (human,type)
MOD_ATT:N-N (human,deficiency)
SUBJ:V_PASS-N (associate,human)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(in) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,mutant)
APPOS (__NODE__,C1069T)
SUBJ:V-N (exhibit,__SP__)
OBJ:V-N (exhibit,palmitoyltransferase)
MOD_ATT:N-ADJ (palmitoyltransferase,__NODE__)
SUBJ:V-N (type,human)