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PubMed:10602116 JSONTXT 12 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T0 395-398 gene:5172 denotes PDS
T1 537-556 disease:C0339789 denotes congenital deafness
T5 1014-1030 disease:C0271829 denotes Pendred syndrome
T7 1014-1030 disease:C0271829 denotes Pendred syndrome
T2 1082-1085 gene:5172 denotes PDS
T4 1082-1085 gene:5730 denotes PDS
T6 1082-1085 gene:5172 denotes PDS
T8 1082-1085 gene:5730 denotes PDS
T10 1082-1085 gene:5172 denotes PDS
T12 1082-1085 gene:5730 denotes PDS
T3 1148-1171 disease:C0262435 denotes congenital hearing loss
T9 1148-1171 disease:C0262435 denotes congenital hearing loss
T11 1245-1259 disease:C0018021 denotes thyroid goiter
T13 1245-1259 disease:C0018021 denotes thyroid goiter
R1 T0 T1 associated_with PDS,congenital deafness
R2 T2 T3 associated_with PDS,congenital hearing loss
R3 T4 T5 associated_with PDS,Pendred syndrome
R4 T6 T7 associated_with PDS,Pendred syndrome
R5 T8 T9 associated_with PDS,congenital hearing loss
R6 T10 T11 associated_with PDS,thyroid goiter
R7 T12 T13 associated_with PDS,thyroid goiter