PubMed:29064616
Annnotations
PubTator4TogoVar
Id | Subject | Object | Predicate | Lexical cue | proteinmutation |
---|---|---|---|---|---|
29064616_0 | 886-893 | ProteinMutation | denotes | p.V246M | rs772145901 |
29064616_1 | 1064-1071 | ProteinMutation | denotes | p.V246M | rs772145901 |
29064616_2 | 1320-1327 | ProteinMutation | denotes | p.E280K | rs114790896 |
29064616_3 | 1332-1339 | ProteinMutation | denotes | p.A705T | rs200188844 |
29064616_4 | 1349-1356 | ProteinMutation | denotes | p.R756C | rs1230549709 |
kaiyin_test
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T9 | 0-16 | PosReg | denotes | Gain-of-function |
T10 | 17-21 | Gene | denotes | HCN2 |
T11 | 22-30 | Var | denotes | variants |
T12 | 42-50 | Disease | denotes | epilepsy |
T5 | 1052-1059 | Var | denotes | p.S632W |
T6 | 1064-1071 | Var | denotes | p.V246M |
T8 | 1119-1163 | MPA | denotes | depolarizing shift in the voltage dependence |
T7 | 1167-1177 | PosReg | denotes | activation |
T1 | 1434-1438 | Gene | denotes | HCN2 |
T2 | 1439-1447 | Var | denotes | variants |
T4 | 1459-1473 | MPA | denotes | susceptibility |
T3 | 1487-1503 | PosReg | denotes | gain-of-function |
R1 | T5 | T7 | CauseOf | p.S632W,activation |
R2 | T6 | T7 | CauseOf | p.V246M,activation |
R3 | T8 | T7 | ThemeOf | depolarizing shift in the voltage dependence,activation |
R4 | T1 | T2 | ThemeOf | HCN2,variants |
R5 | T2 | T3 | CauseOf | variants,gain-of-function |
R6 | T4 | T3 | ThemeOf | susceptibility,gain-of-function |
R7 | T10 | T11 | ThemeOf | HCN2,variants |
R8 | T11 | T9 | CauseOf | variants,Gain-of-function |
R9 | T12 | T9 | ThemeOf | epilepsy,Gain-of-function |
name_no
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T9 | 0-16 | PosReg | denotes | Gain-of-function |
T10 | 17-21 | Gene | denotes | HCN2 |
T11 | 22-30 | Var | denotes | variants |
T12 | 42-50 | Disease | denotes | epilepsy |
T5 | 1052-1059 | Var | denotes | p.S632W |
T6 | 1064-1071 | Var | denotes | p.V246M |
T8 | 1119-1163 | MPA | denotes | depolarizing shift in the voltage dependence |
T7 | 1167-1177 | PosReg | denotes | activation |
T1 | 1434-1438 | Gene | denotes | HCN2 |
T2 | 1439-1447 | Var | denotes | variants |
T4 | 1459-1473 | MPA | denotes | susceptibility |
T3 | 1487-1503 | PosReg | denotes | gain-of-function |
R1 | T5 | T7 | CauseOf | p.S632W,activation |
R2 | T6 | T7 | CauseOf | p.V246M,activation |
R3 | T8 | T7 | ThemeOf | depolarizing shift in the voltage dependence,activation |
R4 | T1 | T2 | ThemeOf | HCN2,variants |
R5 | T2 | T3 | CauseOf | variants,gain-of-function |
R6 | T4 | T3 | ThemeOf | susceptibility,gain-of-function |
R7 | T10 | T11 | ThemeOf | HCN2,variants |
R8 | T11 | T9 | CauseOf | variants,Gain-of-function |
R9 | T12 | T9 | ThemeOf | epilepsy,Gain-of-function |