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Phrase 47 - PMID ?

Familial hypoalphalipoproteinemia in humans is associated with mutant __SP__ __NODE__ protein ( M1091T ) .


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Commentaires :
Analyse 0 
                                                     +---------COMP:V_PASS-N(with)--------+                
                                                     |             +-----MOD_ATT:N-ADJ----+                
                      +---------SUBJ:V_PASS-N--------+             |      +-MOD_ATT:N-ADJ-+                
     +---MOD_ATT:N-N--+---COMP:N-N(in)---+           |             |      |       +MOD_ATT+--APPOS--+      
     |                |                  |           |             |      |       |       |         |      
 Familial hypoalphalipoproteinemia in humans is associated with mutant __SP__ __NODE__ protein ( M1091T ) .
MOD_ATT:N-N (hypoalphalipoproteinemia,familial)
COMP:N-N(in) (hypoalphalipoproteinemia,human)
SUBJ:V_PASS-N (associate,hypoalphalipoproteinemia)
COMP:V_PASS-N(with) (associate,protein)
MOD_ATT:N-ADJ (protein,mutant)
MOD_ATT:N-ADJ (protein,__SP__)
MOD_ATT:N-ADJ (protein,__NODE__)
APPOS (protein,M1091T)
Analyse 1 
                                                             +-----------OBJ:V-N----------+                
                      +---------SUBJ:V_PASS-N--------+-COMP:V_PASS-N(with)+               |                
     +---MOD_ATT:N-N--+---COMP:N-N(in)---+           |       |     +MOD_AT+       +MOD_ATT+--APPOS--+      
     |                |                  |           |       |     |      |       |       |         |      
 Familial hypoalphalipoproteinemia in humans is associated with mutant __SP__ __NODE__ protein ( M1091T ) .
MOD_ATT:N-N (hypoalphalipoproteinemia,familial)
COMP:N-N(in) (hypoalphalipoproteinemia,human)
SUBJ:V_PASS-N (associate,hypoalphalipoproteinemia)
COMP:V_PASS-N(with) (associate,__SP__)
OBJ:V-N (with,protein)
MOD_ATT:N-ADJ (__SP__,mutant)
MOD_ATT:N-ADJ (protein,__NODE__)
APPOS (protein,M1091T)
Analyse 2 
                                                     +-----COMP:V_PASS-N(with)----+                        
                                                     |       +-----------OBJ:V-N----------+                
                      +---------SUBJ:V_PASS-N--------+       |     +-MOD_ATT:N-ADJ+       |                
     +---MOD_ATT:N-N--+---COMP:N-N(in)---+           |       |     |      +MOD_ATT+       +--APPOS--+      
     |                |                  |           |       |     |      |       |       |         |      
 Familial hypoalphalipoproteinemia in humans is associated with mutant __SP__ __NODE__ protein ( M1091T ) .
MOD_ATT:N-N (hypoalphalipoproteinemia,familial)
COMP:N-N(in) (hypoalphalipoproteinemia,human)
SUBJ:V_PASS-N (associate,hypoalphalipoproteinemia)
COMP:V_PASS-N(with) (associate,__NODE__)
OBJ:V-N (with,protein)
MOD_ATT:N-ADJ (__NODE__,mutant)
MOD_ATT:N-ADJ (__NODE__,__SP__)
APPOS (protein,M1091T)