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PubMed:20598714 JSONTXT 19 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 21-26 gene:26580 denotes BSCL2
T2 21-26 gene:26580 denotes BSCL2
T4 21-26 gene:26580 denotes BSCL2
T3 57-98 disease:C1833308 denotes distal hereditary motor neuropathy type V
T1 102-117 disease:C0175693 denotes Silver syndrome
T5 102-117 disease:C2931276 denotes Silver syndrome
T9 131-172 disease:C1833308 denotes Distal hereditary motor neuropathy type V
T17 131-172 disease:C1833308 denotes Distal hereditary motor neuropathy type V
T25 131-172 disease:C1833308 denotes Distal hereditary motor neuropathy type V
T11 174-180 disease:C1833308 denotes dHMN-V
T23 174-180 disease:C1833308 denotes dHMN-V
T7 186-201 disease:C0175693 denotes Silver syndrome
T13 186-201 disease:C2931276 denotes Silver syndrome
T15 186-201 disease:C0175693 denotes Silver syndrome
T19 186-201 disease:C0175693 denotes Silver syndrome
T21 186-201 disease:C2931276 denotes Silver syndrome
T27 186-201 disease:C2931276 denotes Silver syndrome
T12 287-329 gene:10555 denotes Berardinelli-Seip Congenital Lipodystrophy
T14 287-329 gene:10555 denotes Berardinelli-Seip Congenital Lipodystrophy
T22 287-329 gene:10555 denotes Berardinelli-Seip Congenital Lipodystrophy
T24 287-329 gene:10555 denotes Berardinelli-Seip Congenital Lipodystrophy
T6 333-338 gene:26580 denotes BSCL2
T8 333-338 gene:26580 denotes BSCL2
T10 333-338 gene:26580 denotes BSCL2
T26 333-338 gene:26580 denotes BSCL2
T16 348-354 gene:26580 denotes Seipin
T18 348-354 gene:26580 denotes Seipin
T20 348-354 gene:26580 denotes Seipin
T29 522-530 disease:C3714552 denotes weakness
T28 556-561 gene:56955 denotes of 45
R1 T0 T1 associated_with BSCL2,Silver syndrome
R10 T18 T19 associated_with Seipin,Silver syndrome
R11 T20 T21 associated_with Seipin,Silver syndrome
R12 T22 T23 associated_with Berardinelli-Seip Congenital Lipodystrophy,dHMN-V
R13 T24 T25 associated_with Berardinelli-Seip Congenital Lipodystrophy,Distal hereditary motor neuropathy type V
R14 T26 T27 associated_with BSCL2,Silver syndrome
R15 T28 T29 associated_with of 45,weakness
R2 T2 T3 associated_with BSCL2,distal hereditary motor neuropathy type V
R3 T4 T5 associated_with BSCL2,Silver syndrome
R4 T6 T7 associated_with BSCL2,Silver syndrome
R5 T8 T9 associated_with BSCL2,Distal hereditary motor neuropathy type V
R6 T10 T11 associated_with BSCL2,dHMN-V
R7 T12 T13 associated_with Berardinelli-Seip Congenital Lipodystrophy,Silver syndrome
R8 T14 T15 associated_with Berardinelli-Seip Congenital Lipodystrophy,Silver syndrome
R9 T16 T17 associated_with Seipin,Distal hereditary motor neuropathy type V