Validation pour Ingenuity432

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Ingenuity432

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 76 - PMID ?

Tangier disease in humans is associated with missense mutant SP NODE gene ( A5338C with its transmembrane domain 2 mutated ) .

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

Commentaires :

Analyse 0

                                   +---------COMP:V_PASS-N(with)---------+                                                             
                                   |              +-----MOD_ATT:N-ADJ----+                                                             
            +-----SUBJ:V_PASS-N----+              |       +-MOD_ATT:N-ADJ+                                            +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |              |       |      +MOD_ATT+                                 +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |                                 |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,missense)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 1

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +---------COMP:V_PASS-N(with)---------+                                            |                
                                   |              +-----MOD_ATT:N-ADJ----+                                            |                
            +-----SUBJ:V_PASS-N----+              |       +-MOD_ATT:N-ADJ+                                            +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |              |       |      +MOD_ATT+                                 +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |                                 |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(with) (associate,domain)
MOD_ATT:N-ADJ (__NODE__,missense)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 2

                                   +-----COMP:V_PASS-N(with)-----+                                                                     
            +-----SUBJ:V_PASS-N----+              +-MOD_ATT:N-ADJ+                                                    +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |              |       +MOD_AT+                                         +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |                                         |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 3

                                   +---------COMP:V_PASS-N(with)---------+                                                             
                                   |              +-----MOD_ATT:N-ADJ----+                                                             
            +-----SUBJ:V_PASS-N----+              |       +-MOD_ATT:N-ADJ+                    +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |              |       |      +MOD_ATT+                    |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |                    |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
MOD_ATT:N-ADJ (__NODE__,missense)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 4

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +-----COMP:V_PASS-N(with)-----+                                                    |                
            +-----SUBJ:V_PASS-N----+              +-MOD_ATT:N-ADJ+                                                    +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |              |       +MOD_AT+                                         +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |                                         |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(with) (associate,domain)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 5

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +---------COMP:V_PASS-N(with)---------+                                            |                
                                   |              +-----MOD_ATT:N-ADJ----+                                            |                
            +-----SUBJ:V_PASS-N----+              |       +-MOD_ATT:N-ADJ+                    +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |              |       |      +MOD_ATT+                    |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |                    |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(with) (associate,domain)
MOD_ATT:N-ADJ (__NODE__,missense)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 6

                                   +-----COMP:V_PASS-N(with)-----+                                                                     
                                   |       +-----------OBJ:V-N-----------+                                                             
            +-----SUBJ:V_PASS-N----+       |      +-MOD_ATT:N-ADJ+       |                                            +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |       |      |       +MOD_AT+       |                                 +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |                                 |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 7

                                   +-----COMP:V_PASS-N(with)-----+                                                                     
            +-----SUBJ:V_PASS-N----+              +-MOD_ATT:N-ADJ+                            +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |              |       +MOD_AT+                            |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |                            |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 8

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +-----COMP:V_PASS-N(with)-----+                                                    |                
                                   |       +-----------OBJ:V-N-----------+                                            |                
            +-----SUBJ:V_PASS-N----+       |      +-MOD_ATT:N-ADJ+       |                                            +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |       |      |       +MOD_AT+       |                                 +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |                                 |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(with) (associate,domain)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 9

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +-----COMP:V_PASS-N(with)-----+                                                    |                
            +-----SUBJ:V_PASS-N----+              +-MOD_ATT:N-ADJ+                            +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |              |       +MOD_AT+                            |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |                            |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(with) (associate,domain)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 10

                                   +-----COMP:V_PASS-N(with)-----+                                                                     
                                   |       +-----------OBJ:V-N-----------+                                                             
            +-----SUBJ:V_PASS-N----+       |      +-MOD_ATT:N-ADJ+       |                    +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |       |      |       +MOD_AT+       |                    |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |                    |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 11

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +-----------------COMP:V_PASS-N(with)----------------+                             |                
                                   |              +--------MOD_ATT:N-ADJ--------+       |                             |                
                                   |              |       +----MOD_ATT:N-ADJ----+       |                             |                
            +-----SUBJ:V_PASS-N----+              |       |      +-MOD_ATT:N-ADJ+       |                             +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |              |       |      |       +MOD_AT+MOD_ATT+                  +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |      |       |                  |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,A5338C)
COMP:V_PASS-N(with) (associate,domain)
MOD_ATT:N-ADJ (gene,missense)
MOD_ATT:N-ADJ (gene,mutant)
MOD_ATT:N-ADJ (gene,__SP__)
MOD_ATT:N-ADJ (gene,__NODE__)
MOD_ATT:N-N (A5338C,gene)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 12

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +-----COMP:V_PASS-N(with)-----+                                                    |                
                                   |       +-----------OBJ:V-N-----------+                                            |                
            +-----SUBJ:V_PASS-N----+       |      +-MOD_ATT:N-ADJ+       |                    +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |       |      |       +MOD_AT+       |                    |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |                    |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(with) (associate,domain)
OBJ:V-N (with,__NODE__)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 13

                                   +-----------------COMP:V_PASS-N(with)----------------+                                              
                                   |              +--------MOD_ATT:N-ADJ--------+       |                                              
                                   |              |       +----MOD_ATT:N-ADJ----+       |                                              
            +-----SUBJ:V_PASS-N----+              |       |      +-MOD_ATT:N-ADJ+       |                             +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |              |       |      |       +MOD_AT+MOD_ATT+                  +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |      |       |                  |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,A5338C)
MOD_ATT:N-ADJ (gene,missense)
MOD_ATT:N-ADJ (gene,mutant)
MOD_ATT:N-ADJ (gene,__SP__)
MOD_ATT:N-ADJ (gene,__NODE__)
MOD_ATT:N-N (A5338C,gene)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 14

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   +-----------------COMP:V_PASS-N(with)----------------+                             |                
                                   |              +--------MOD_ATT:N-ADJ--------+       |                             |                
                                   |              |       +----MOD_ATT:N-ADJ----+       |                             |                
            +-----SUBJ:V_PASS-N----+              |       |      +-MOD_ATT:N-ADJ+       |     +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |              |       |      |       +MOD_AT+MOD_ATT+     |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |              |       |      |       |      |       |     |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,A5338C)
COMP:V_PASS-N(with) (associate,domain)
MOD_ATT:N-ADJ (gene,missense)
MOD_ATT:N-ADJ (gene,mutant)
MOD_ATT:N-ADJ (gene,__SP__)
MOD_ATT:N-ADJ (gene,__NODE__)
MOD_ATT:N-N (A5338C,gene)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 15

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   |       +-------------------OBJ:V-N------------------+                             |                
                                   +-----COMP:V_PASS-N(with)-----+                      |                             |                
            +-----SUBJ:V_PASS-N----+       |      +-MOD_ATT:N-ADJ+                      |                             +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |       |      |       +MOD_AT+       +MOD_AT+MOD_ATT+                  +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |      |       |                  |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(with) (associate,domain)
OBJ:V-N (with,A5338C)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (gene,__NODE__)
MOD_ATT:N-N (A5338C,gene)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 16

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   |       +-------------------OBJ:V-N------------------+                             |                
                                   +---------COMP:V_PASS-N(with)---------+              |                             |                
                                   |       |      +-----MOD_ATT:N-ADJ----+              |                             |                
            +-----SUBJ:V_PASS-N----+       |      |       +-MOD_ATT:N-ADJ+              |                             +-OBJ:V-N+       
    +MOD_ATT+COMP:N-N(i+           |       |      |       |      +MOD_ATT+      +MOD_ATT+                  +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |      |       |                  |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(with) (associate,domain)
OBJ:V-N (with,A5338C)
MOD_ATT:N-ADJ (__NODE__,missense)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
MOD_ATT:N-N (A5338C,gene)
MOD_ATT:N-ADJ (domain,transmembrane)
OBJ:V-N (mutate,domain)
SUBJ:V-N (mutate,2)

Analyse 17

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   |       +-------------------OBJ:V-N------------------+                             |                
                                   +-----COMP:V_PASS-N(with)-----+                      |                             |                
            +-----SUBJ:V_PASS-N----+       |      +-MOD_ATT:N-ADJ+                      |     +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |       |      |       +MOD_AT+       +MOD_AT+MOD_ATT+     |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |      |       |     |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__SP__)
COMP:V_PASS-N(with) (associate,domain)
OBJ:V-N (with,A5338C)
MOD_ATT:N-ADJ (__SP__,missense)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (gene,__NODE__)
MOD_ATT:N-N (A5338C,gene)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)

Analyse 18

                                   +--------------------------------COMP:V_PASS-N(with)-------------------------------+                
                                   |       +-------------------OBJ:V-N------------------+                             |                
                                   +---------COMP:V_PASS-N(with)---------+              |                             |                
                                   |       |      +-----MOD_ATT:N-ADJ----+              |                             |                
            +-----SUBJ:V_PASS-N----+       |      |       +-MOD_ATT:N-ADJ+              |     +----------OBJ:V-N----------+            
    +MOD_ATT+COMP:N-N(i+           |       |      |       |      +MOD_ATT+      +MOD_ATT+     |            +MOD_ATT:N-+   +SUBJ+       
    |       |          |           |       |      |       |      |       |      |       |     |            |          |   |    |       
 Tangier disease in humans is associated with missense mutant __SP__ __NODE__ gene ( A5338C with its transmembrane domain 2 mutated ) .
MOD_ATT:N-N (disease,tangy)
COMP:N-N(in) (disease,human)
SUBJ:V_PASS-N (associate,disease)
COMP:V_PASS-N(with) (associate,__NODE__)
COMP:V_PASS-N(with) (associate,domain)
OBJ:V-N (with,A5338C)
MOD_ATT:N-ADJ (__NODE__,missense)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
MOD_ATT:N-N (A5338C,gene)
OBJ:V-N (with,2)
MOD_ATT:N-ADJ (domain,transmembrane)
SUBJ:V_PASS-N (mutate,2)