PubMed:28817352
Annnotations
kaiyin_test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T2 | 196-205 | Var | denotes | mutations |
T1 | 209-217 | Gene | denotes | ARHGAP29 |
T18 | 218-228 | Reg | denotes | associated |
T4 | 256-262 | Disease | denotes | NSCL/P |
T5 | 419-446 | Var | denotes | single-nucleotide variation |
T6 | 450-458 | Gene | denotes | ARHGAP29 |
T7 | 501-506 | Var | denotes | K326X |
T8 | 533-549 | NegReg | denotes | loss-of-function |
T9 | 1718-1721 | NegReg | denotes | LoF |
T10 | 1722-1730 | Var | denotes | variants |
T11 | 1734-1742 | Gene | denotes | Arhgap29 |
T12 | 1743-1752 | PosReg | denotes | increases |
T13 | 1757-1849 | CPA | denotes | incidence and length of oral adhesions at a critical time point during orofacial development |
T14 | 1882-1885 | NegReg | denotes | LoF |
T15 | 1906-1920 | Var | denotes | K326X mutation |
T16 | 1971-1979 | Gene | denotes | Arhgap29 |
T17 | 1990-2014 | CPA | denotes | craniofacial development |
R10 | T10 | T9 | CauseOf | variants,LoF |
R11 | T11 | T10 | ThemeOf | Arhgap29,variants |
R12 | T10 | T12 | CauseOf | variants,increases |
R13 | T13 | T12 | ThemeOf | incidence and length of oral adhesions at a critical time point during orofacial development,increases |
R14 | T2 | T18 | CauseOf | mutations,associated |
R15 | T4 | T18 | ThemeOf | NSCL/P,associated |
R3 | T1 | T2 | ThemeOf | ARHGAP29,mutations |
R4 | T5 | T8 | CauseOf | single-nucleotide variation,loss-of-function |
R5 | T7 | T5 | ThemeOf | K326X,single-nucleotide variation |
R6 | T6 | T5 | ThemeOf | ARHGAP29,single-nucleotide variation |
R7 | T15 | T14 | CauseOf | K326X mutation,LoF |
R8 | T17 | T14 | ThemeOf | craniofacial development,LoF |
R9 | T16 | T15 | ThemeOf | Arhgap29,K326X mutation |
name_no
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T2 | 196-205 | Var | denotes | mutations |
T1 | 209-217 | Gene | denotes | ARHGAP29 |
T18 | 218-228 | Reg | denotes | associated |
T4 | 256-262 | Disease | denotes | NSCL/P |
T5 | 419-446 | Var | denotes | single-nucleotide variation |
T6 | 450-458 | Gene | denotes | ARHGAP29 |
T7 | 501-506 | Var | denotes | K326X |
T8 | 533-549 | NegReg | denotes | loss-of-function |
T9 | 1718-1721 | NegReg | denotes | LoF |
T10 | 1722-1730 | Var | denotes | variants |
T11 | 1734-1742 | Gene | denotes | Arhgap29 |
T12 | 1743-1752 | PosReg | denotes | increases |
T13 | 1757-1849 | CPA | denotes | incidence and length of oral adhesions at a critical time point during orofacial development |
T14 | 1882-1885 | NegReg | denotes | LoF |
T15 | 1906-1920 | Var | denotes | K326X mutation |
T16 | 1971-1979 | Gene | denotes | Arhgap29 |
T17 | 1990-2014 | CPA | denotes | craniofacial development |
R10 | T10 | T9 | CauseOf | variants,LoF |
R11 | T11 | T10 | ThemeOf | Arhgap29,variants |
R12 | T10 | T12 | CauseOf | variants,increases |
R13 | T13 | T12 | ThemeOf | incidence and length of oral adhesions at a critical time point during orofacial development,increases |
R14 | T2 | T18 | CauseOf | mutations,associated |
R15 | T4 | T18 | ThemeOf | NSCL/P,associated |
R3 | T1 | T2 | ThemeOf | ARHGAP29,mutations |
R4 | T5 | T8 | CauseOf | single-nucleotide variation,loss-of-function |
R5 | T7 | T5 | ThemeOf | K326X,single-nucleotide variation |
R6 | T6 | T5 | ThemeOf | ARHGAP29,single-nucleotide variation |
R7 | T15 | T14 | CauseOf | K326X mutation,LoF |
R8 | T17 | T14 | ThemeOf | craniofacial development,LoF |
R9 | T16 | T15 | ThemeOf | Arhgap29,K326X mutation |