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PubMed:30702381 JSONTXT

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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