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PubMed:28807867 JSON TXT 28 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id	Subject	Object	Predicate	Lexical cue
T3	163-184	Disease	denotes	Pitt-Hopkins syndrome
T4	306-315	Reg	denotes	caused by
T2	316-334	Var	denotes	haploinsufficiency
T1	342-346	Gene	denotes	TCF4
T5	879-887	Var	denotes	variants
T6	888-898	NegReg	denotes	disrupting
T7	899-903	Gene	denotes	TCF4
T9	924-931	Disease	denotes	mild ID
T10	974-984	Var	denotes	frameshift
T11	985-992	Reg	denotes	causing
T12	993-1014	Var	denotes	partial gene deletion
T13	1041-1045	Gene	denotes	TCF4
T15	1066-1070	Reg	denotes	with
T14	1071-1078	Disease	denotes	mild ID
T16	1163-1173	Var	denotes	c.520C > T
T18	1227-1231	Reg	denotes	with
T17	1269-1273	Disease	denotes	PTHS
R1	T2	T4	CauseOf	haploinsufficiency,caused by
R10	T12	T15	CauseOf	partial gene deletion,with
R11	T14	T15	ThemeOf	mild ID,with
R12	T16	T18	CauseOf	c.520C > T,with
R13	T17	T18	ThemeOf	PTHS,with
R2	T3	T4	ThemeOf	Pitt-Hopkins syndrome,caused by
R3	T1	T2	ThemeOf	TCF4,haploinsufficiency
R4	T5	T6	CauseOf	variants,disrupting
R5	T7	T5	ThemeOf	TCF4,variants
R6	T9	T6	ThemeOf	mild ID,disrupting
R7	T10	T11	CauseOf	frameshift,causing
R8	T12	T11	ThemeOf	partial gene deletion,causing
R9	T13	T12	ThemeOf	TCF4,partial gene deletion