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PubMed:28817352 JSONTXT 29 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T2 196-205 Var denotes mutations
T1 209-217 Gene denotes ARHGAP29
T18 218-228 Reg denotes associated
T4 256-262 Disease denotes NSCL/P
T5 419-446 Var denotes single-nucleotide variation
T6 450-458 Gene denotes ARHGAP29
T7 501-506 Var denotes K326X
T8 533-549 NegReg denotes loss-of-function
T9 1718-1721 NegReg denotes LoF
T10 1722-1730 Var denotes variants
T11 1734-1742 Gene denotes Arhgap29
T12 1743-1752 PosReg denotes increases
T13 1757-1849 CPA denotes incidence and length of oral adhesions at a critical time point during orofacial development
T14 1882-1885 NegReg denotes LoF
T15 1906-1920 Var denotes K326X mutation
T16 1971-1979 Gene denotes Arhgap29
T17 1990-2014 CPA denotes craniofacial development
R10 T10 T9 CauseOf variants,LoF
R11 T11 T10 ThemeOf Arhgap29,variants
R12 T10 T12 CauseOf variants,increases
R13 T13 T12 ThemeOf incidence and length of oral adhesions at a critical time point during orofacial development,increases
R14 T2 T18 CauseOf mutations,associated
R15 T4 T18 ThemeOf NSCL/P,associated
R3 T1 T2 ThemeOf ARHGAP29,mutations
R4 T5 T8 CauseOf single-nucleotide variation,loss-of-function
R5 T7 T5 ThemeOf K326X,single-nucleotide variation
R6 T6 T5 ThemeOf ARHGAP29,single-nucleotide variation
R7 T15 T14 CauseOf K326X mutation,LoF
R8 T17 T14 ThemeOf craniofacial development,LoF
R9 T16 T15 ThemeOf Arhgap29,K326X mutation