PubMed:30702381
Annnotations
AGAC_v3
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T6 | 142-160 | Disease | denotes | Uniparental disomy |
T3 | 1113-1118 | Gene | denotes | F13A1 |
T4 | 1152-1171 | Var | denotes | duplicate mutations |
T5 | 1236-1243 | Reg | denotes | case of |
T2 | 1271-1274 | Disease | denotes | UPD |
T1 | 1331-1347 | Disease | denotes | FXIII deficiency |
R4 | T1 | T5 | ThemeOf | FXIII deficiency,case of |
R3 | T2 | T5 | ThemeOf | UPD,case of |
R2 | T4 | T5 | CauseOf | duplicate mutations,case of |
R1 | T3 | T4 | ThemeOf | F13A1,duplicate mutations |
AGAC-FULL-201905
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T6 | 142-160 | Disease | denotes | Uniparental disomy |
T3 | 1113-1118 | Gene | denotes | F13A1 |
T4 | 1152-1171 | Var | denotes | duplicate mutations |
T5 | 1236-1243 | Reg | denotes | case of |
T2 | 1271-1274 | Disease | denotes | UPD |
T1 | 1331-1347 | Disease | denotes | FXIII deficiency |
R1 | T3 | T4 | ThemeOf | F13A1,duplicate mutations |
R2 | T4 | T5 | CauseOf | duplicate mutations,case of |
R3 | T2 | T5 | ThemeOf | UPD,case of |
R4 | T1 | T5 | ThemeOf | FXIII deficiency,case of |
AGAC2_PubMed7000
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1331-1347 | Disease | denotes | FXIII deficiency |
T2 | 1271-1274 | Disease | denotes | UPD |
T3 | 1113-1118 | Gene | denotes | F13A1 |
T4 | 1152-1171 | Var | denotes | duplicate mutations |
T5 | 1236-1243 | Reg | denotes | case of |
T6 | 142-160 | Disease | denotes | Uniparental disomy |
R1 | T3 | T4 | ThemeOf | F13A1,duplicate mutations |
R2 | T4 | T5 | CauseOf | duplicate mutations,case of |
R3 | T2 | T5 | ThemeOf | UPD,case of |
R4 | T1 | T5 | ThemeOf | FXIII deficiency,case of |
AGAC_answer
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T6 | 142-160 | Disease | denotes | Uniparental disomy |
T3 | 1113-1118 | Gene | denotes | F13A1 |
T4 | 1152-1171 | Var | denotes | duplicate mutations |
T5 | 1236-1243 | Reg | denotes | case of |
T2 | 1271-1274 | Disease | denotes | UPD |
T1 | 1331-1347 | Disease | denotes | FXIII deficiency |
R1 | T3 | T4 | ThemeOf | F13A1,duplicate mutations |
R2 | T4 | T5 | CauseOf | duplicate mutations,case of |
R3 | T2 | T5 | ThemeOf | UPD,case of |
R4 | T1 | T5 | ThemeOf | FXIII deficiency,case of |