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PubMed:29330547 JSONTXT

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kaiyin_test

Id Subject Object Predicate Lexical cue
T12 27-31 Gene denotes PIGN
T11 65-73 Var denotes deletion
T7 556-585 Var denotes biallelic truncating variants
T6 589-593 Gene denotes PIGN
T9 697-707 Reg denotes identified
T8 770-772 Disease denotes FS
T1 796-800 Gene denotes PIGN
T2 812-820 Var denotes missense
T3 824-841 Var denotes compound missense
T10 847-857 MPA denotes truncating
T4 864-869 Reg denotes cause
T5 870-929 Disease denotes multiple congenital anomalies-hypotonia-seizures syndrome 1
R1 T1 T2 ThemeOf PIGN,missense
R10 T3 T10 CauseOf compound missense,truncating
R11 T10 T4 CauseOf truncating,cause
R2 T1 T3 ThemeOf PIGN,compound missense
R3 T5 T4 ThemeOf multiple congenital anomalies-hypotonia-seizures syndrome 1,cause
R6 T6 T7 ThemeOf PIGN,biallelic truncating variants
R7 T7 T9 CauseOf biallelic truncating variants,identified
R8 T8 T9 ThemeOf FS,identified
R9 T2 T10 CauseOf missense,truncating

name_no

Id Subject Object Predicate Lexical cue
T12 27-31 Gene denotes PIGN
T11 65-73 Var denotes deletion
T7 556-585 Var denotes biallelic truncating variants
T6 589-593 Gene denotes PIGN
T9 697-707 Reg denotes identified
T8 770-772 Disease denotes FS
T1 796-800 Gene denotes PIGN
T2 812-820 Var denotes missense
T3 824-841 Var denotes compound missense
T10 847-857 MPA denotes truncating
T4 864-869 Reg denotes cause
T5 870-929 Disease denotes multiple congenital anomalies-hypotonia-seizures syndrome 1
R1 T1 T2 ThemeOf PIGN,missense
R10 T3 T10 CauseOf compound missense,truncating
R11 T10 T4 CauseOf truncating,cause
R2 T1 T3 ThemeOf PIGN,compound missense
R3 T5 T4 ThemeOf multiple congenital anomalies-hypotonia-seizures syndrome 1,cause
R6 T6 T7 ThemeOf PIGN,biallelic truncating variants
R7 T7 T9 CauseOf biallelic truncating variants,identified
R8 T8 T9 ThemeOf FS,identified
R9 T2 T10 CauseOf missense,truncating