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PubMed:28488085 JSONTXT

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kaiyin_test

Id Subject Object Predicate Lexical cue
T1 6-22 NegReg denotes loss of function
T2 23-31 Var denotes mutation
T3 35-40 Gene denotes KRIT1
T4 49-64 Reg denotes associated with
T5 88-131 Disease denotes cerebral and spinal cavernous malformations
T6 209-246 Disease denotes Cerebrospinal cavernous malformations
T8 1355-1360 Gene denotes KRIT1
T7 1390-1406 Var denotes c.1535_1536delTG
T9 1434-1442 Reg denotes leads to
T10 1445-1455 Var denotes frameshift
T11 1463-1483 MPA denotes premature stop codon
T12 1532-1548 NegReg denotes loss of function
T13 1556-1569 Protein denotes KRIT1 protein
T14 1641-1657 NegReg denotes loss of function
T15 1658-1666 Var denotes mutation
T16 1670-1675 Gene denotes KRIT1
T17 1686-1701 Reg denotes associated with
T18 1737-1741 Disease denotes CCMs
R1 T2 T1 CauseOf mutation,loss of function
R10 T13 T12 ThemeOf KRIT1 protein,loss of function
R11 T15 T14 CauseOf mutation,loss of function
R12 T16 T15 ThemeOf KRIT1,mutation
R13 T15 T17 CauseOf mutation,associated with
R14 T18 T17 ThemeOf CCMs,associated with
R2 T3 T2 ThemeOf KRIT1,mutation
R3 T2 T4 CauseOf mutation,associated with
R4 T5 T4 ThemeOf cerebral and spinal cavernous malformations,associated with
R5 T7 T9 CauseOf c.1535_1536delTG,leads to
R6 T10 T9 ThemeOf frameshift,leads to
R7 T11 T9 ThemeOf premature stop codon,leads to
R8 T8 T7 ThemeOf KRIT1,c.1535_1536delTG
R9 T7 T12 CauseOf c.1535_1536delTG,loss of function

name_no

Id Subject Object Predicate Lexical cue
T1 6-22 NegReg denotes loss of function
T2 23-31 Var denotes mutation
T3 35-40 Gene denotes KRIT1
T4 49-64 Reg denotes associated with
T5 88-131 Disease denotes cerebral and spinal cavernous malformations
T6 209-246 Disease denotes Cerebrospinal cavernous malformations
T8 1355-1360 Gene denotes KRIT1
T7 1390-1406 Var denotes c.1535_1536delTG
T9 1434-1442 Reg denotes leads to
T10 1445-1455 Var denotes frameshift
T11 1463-1483 MPA denotes premature stop codon
T12 1532-1548 NegReg denotes loss of function
T13 1556-1569 Protein denotes KRIT1 protein
T14 1641-1657 NegReg denotes loss of function
T15 1658-1666 Var denotes mutation
T16 1670-1675 Gene denotes KRIT1
T17 1686-1701 Reg denotes associated with
T18 1737-1741 Disease denotes CCMs
R1 T2 T1 CauseOf mutation,loss of function
R10 T13 T12 ThemeOf KRIT1 protein,loss of function
R11 T15 T14 CauseOf mutation,loss of function
R12 T16 T15 ThemeOf KRIT1,mutation
R13 T15 T17 CauseOf mutation,associated with
R14 T18 T17 ThemeOf CCMs,associated with
R2 T3 T2 ThemeOf KRIT1,mutation
R3 T2 T4 CauseOf mutation,associated with
R4 T5 T4 ThemeOf cerebral and spinal cavernous malformations,associated with
R5 T7 T9 CauseOf c.1535_1536delTG,leads to
R6 T10 T9 ThemeOf frameshift,leads to
R7 T11 T9 ThemeOf premature stop codon,leads to
R8 T8 T7 ThemeOf KRIT1,c.1535_1536delTG
R9 T7 T12 CauseOf c.1535_1536delTG,loss of function