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kaiyin_test

Id Subject Object Predicate Lexical cue
T2 15-24 Var denotes mutations
T1 54-60 Gene denotes KCNJ10
T3 73-78 Gene denotes KCNT1
T4 80-90 Reg denotes associated
T5 113-121 Disease denotes seizures
T6 126-150 Disease denotes neurodevelopmental delay
T8 1008-1014 Gene denotes KCNJ10
T7 1015-1023 Var denotes mutation
T9 1033-1044 Reg denotes resulted in
T10 1055-1067 Var denotes substitution
T12 1258-1265 NegReg denotes reduced
T11 1266-1284 MPA denotes protein expression
T13 1292-1300 Var denotes mutation
T16 1590-1606 NegReg denotes loss-of-function
T17 1607-1615 Var denotes mutation
T18 1663-1671 Var denotes mutation
T14 1695-1705 Reg denotes results in
T15 1708-1721 Disease denotes fatal disease
R1 T2 T4 CauseOf mutations,associated
R10 T11 T12 ThemeOf protein expression,reduced
R11 T17 T16 CauseOf mutation,loss-of-function
R12 T18 T17 ThemeOf mutation,mutation
R13 T17 T14 CauseOf mutation,results in
R14 T15 T14 ThemeOf fatal disease,results in
R2 T5 T4 ThemeOf seizures,associated
R3 T1 T2 ThemeOf KCNJ10,mutations
R4 T3 T2 ThemeOf KCNT1,mutations
R5 T6 T4 ThemeOf neurodevelopmental delay,associated
R6 T8 T7 ThemeOf KCNJ10,mutation
R7 T7 T9 CauseOf mutation,resulted in
R8 T10 T9 ThemeOf substitution,resulted in
R9 T13 T12 CauseOf mutation,reduced

name_no

Id Subject Object Predicate Lexical cue
T2 15-24 Var denotes mutations
T1 54-60 Gene denotes KCNJ10
T3 73-78 Gene denotes KCNT1
T4 80-90 Reg denotes associated
T5 113-121 Disease denotes seizures
T6 126-150 Disease denotes neurodevelopmental delay
T8 1008-1014 Gene denotes KCNJ10
T7 1015-1023 Var denotes mutation
T9 1033-1044 Reg denotes resulted in
T10 1055-1067 Var denotes substitution
T12 1258-1265 NegReg denotes reduced
T11 1266-1284 MPA denotes protein expression
T13 1292-1300 Var denotes mutation
T16 1590-1606 NegReg denotes loss-of-function
T17 1607-1615 Var denotes mutation
T18 1663-1671 Var denotes mutation
T14 1695-1705 Reg denotes results in
T15 1708-1721 Disease denotes fatal disease
R1 T2 T4 CauseOf mutations,associated
R10 T11 T12 ThemeOf protein expression,reduced
R11 T17 T16 CauseOf mutation,loss-of-function
R12 T18 T17 ThemeOf mutation,mutation
R13 T17 T14 CauseOf mutation,results in
R14 T15 T14 ThemeOf fatal disease,results in
R2 T5 T4 ThemeOf seizures,associated
R3 T1 T2 ThemeOf KCNJ10,mutations
R4 T3 T2 ThemeOf KCNT1,mutations
R5 T6 T4 ThemeOf neurodevelopmental delay,associated
R6 T8 T7 ThemeOf KCNJ10,mutation
R7 T7 T9 CauseOf mutation,resulted in
R8 T10 T9 ThemeOf substitution,resulted in
R9 T13 T12 CauseOf mutation,reduced