PubMed:29330547
Annnotations
kaiyin_test
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 |
name_no
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 |