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PubMed:11778160 JSONTXT 6 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function

Id Subject Object Predicate Lexical cue
T2 38-44 gene:3239 denotes HOXD13
T0 49-53 gene:344191 denotes EVX2
T1 61-75 disease:C2699746 denotes synpolydactyly
T3 61-75 disease:C2699746 denotes synpolydactyly
T4 226-232 gene:3239 denotes HOXD13
T6 226-232 gene:3239 denotes HOXD13
T8 226-232 gene:3239 denotes HOXD13
T5 264-281 disease:C0206762 denotes limb malformation
T7 282-296 disease:C2699746 denotes synpolydactyly
T9 298-301 disease:C2699746 denotes SPD
T11 907-917 disease:C0432028 denotes split foot
T10 970-974 gene:3230 denotes HOXD
R1 T0 T1 associated_with EVX2,synpolydactyly
R2 T2 T3 associated_with HOXD13,synpolydactyly
R3 T4 T5 associated_with HOXD13,limb malformation
R4 T6 T7 associated_with HOXD13,synpolydactyly
R5 T8 T9 associated_with HOXD13,SPD
R6 T10 T11 associated_with HOXD,split foot