Id |
Subject |
Object |
Predicate |
Lexical cue |
T12 |
27-31 |
Gene |
denotes |
PIGN |
T11 |
65-73 |
Var |
denotes |
deletion |
T7 |
556-585 |
Var |
denotes |
biallelic truncating variants |
T6 |
589-593 |
Gene |
denotes |
PIGN |
T9 |
697-707 |
Reg |
denotes |
identified |
T8 |
770-772 |
Disease |
denotes |
FS |
T1 |
796-800 |
Gene |
denotes |
PIGN |
T2 |
812-820 |
Var |
denotes |
missense |
T3 |
824-841 |
Var |
denotes |
compound missense |
T10 |
847-857 |
MPA |
denotes |
truncating |
T4 |
864-869 |
Reg |
denotes |
cause |
T5 |
870-929 |
Disease |
denotes |
multiple congenital anomalies-hypotonia-seizures syndrome 1 |
R1 |
T1 |
T2 |
ThemeOf |
PIGN,missense |
R10 |
T3 |
T10 |
CauseOf |
compound missense,truncating |
R11 |
T10 |
T4 |
CauseOf |
truncating,cause |
R2 |
T1 |
T3 |
ThemeOf |
PIGN,compound missense |
R3 |
T5 |
T4 |
ThemeOf |
multiple congenital anomalies-hypotonia-seizures syndrome 1,cause |
R6 |
T6 |
T7 |
ThemeOf |
PIGN,biallelic truncating variants |
R7 |
T7 |
T9 |
CauseOf |
biallelic truncating variants,identified |
R8 |
T8 |
T9 |
ThemeOf |
FS,identified |
R9 |
T2 |
T10 |
CauseOf |
missense,truncating |