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PubMed:28741757 JSONTXT

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kaiyin_test

Id Subject Object Predicate Lexical cue
T3 11-27 Var denotes missense variant
T1 35-40 Gene denotes FOXP2
T2 45-50 Gene denotes FOXP1
T4 73-79 Reg denotes causes
T5 89-117 Disease denotes neurodevelopmental disorders
T6 289-298 Var denotes mutations
T7 302-307 Gene denotes FOXP2
T8 308-315 Reg denotes lead to
T9 360-387 Disease denotes childhood apraxia of speech
T10 419-424 Gene denotes FOXP1
T11 425-433 Var denotes variants
T15 434-442 Reg denotes includes
T12 487-513 Disease denotes global developmental delay
T13 515-538 Disease denotes intellectual disability
T14 544-570 Disease denotes speech/language impairment
R1 T3 T4 CauseOf missense variant,causes
R10 T12 T15 ThemeOf global developmental delay,includes
R11 T13 T15 ThemeOf intellectual disability,includes
R12 T14 T15 ThemeOf speech/language impairment,includes
R2 T5 T4 ThemeOf neurodevelopmental disorders,causes
R3 T1 T3 ThemeOf FOXP2,missense variant
R4 T2 T3 ThemeOf FOXP1,missense variant
R5 T6 T8 CauseOf mutations,lead to
R6 T7 T6 ThemeOf FOXP2,mutations
R7 T9 T8 ThemeOf childhood apraxia of speech,lead to
R8 T10 T11 ThemeOf FOXP1,variants
R9 T11 T15 CauseOf variants,includes

name_no

Id Subject Object Predicate Lexical cue
T3 11-27 Var denotes missense variant
T1 35-40 Gene denotes FOXP2
T2 45-50 Gene denotes FOXP1
T4 73-79 Reg denotes causes
T5 89-117 Disease denotes neurodevelopmental disorders
T6 289-298 Var denotes mutations
T7 302-307 Gene denotes FOXP2
T8 308-315 Reg denotes lead to
T9 360-387 Disease denotes childhood apraxia of speech
T10 419-424 Gene denotes FOXP1
T11 425-433 Var denotes variants
T15 434-442 Reg denotes includes
T12 487-513 Disease denotes global developmental delay
T13 515-538 Disease denotes intellectual disability
T14 544-570 Disease denotes speech/language impairment
R1 T3 T4 CauseOf missense variant,causes
R10 T12 T15 ThemeOf global developmental delay,includes
R11 T13 T15 ThemeOf intellectual disability,includes
R12 T14 T15 ThemeOf speech/language impairment,includes
R2 T5 T4 ThemeOf neurodevelopmental disorders,causes
R3 T1 T3 ThemeOf FOXP2,missense variant
R4 T2 T3 ThemeOf FOXP1,missense variant
R5 T6 T8 CauseOf mutations,lead to
R6 T7 T6 ThemeOf FOXP2,mutations
R7 T9 T8 ThemeOf childhood apraxia of speech,lead to
R8 T10 T11 ThemeOf FOXP1,variants
R9 T11 T15 CauseOf variants,includes