PubMed:11778160 JSONTXT 6 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
11778160-0#32#37#gene3235 32-37 gene3235 denotes HOXD9
11778160-0#38#44#gene3239 38-44 gene3239 denotes HOXD13
11778160-0#49#53#gene344191 49-53 gene344191 denotes EVX2
11778160-0#61#75#diseaseC2699746 61-75 diseaseC2699746 denotes synpolydactyly
11778160-2#24#30#gene3239 226-232 gene3239 denotes HOXD13
11778160-2#62#79#diseaseC0206762 264-281 diseaseC0206762 denotes limb malformation
11778160-2#96#99#diseaseC2609259 298-301 diseaseC2609259 denotes SPD
11778160-7#37#47#diseaseC0432028 907-917 diseaseC0432028 denotes split foot
11778160-7#100#104#gene3230 970-974 gene3230 denotes HOXD
11778160-8#57#61#gene3230 1090-1094 gene3230 denotes HOXD
11778160-8#79#83#diseaseC2699510 1112-1116 diseaseC2699510 denotes SHFM
11778160-8#79#83#diseaseC2699510 1112-1116 diseaseC2699510 denotes SHFM
11778160-8#88#91#diseaseC2609259 1121-1124 diseaseC2609259 denotes SPD
11778160-8#88#91#diseaseC2609259 1121-1124 diseaseC2609259 denotes SPD
11778160-8#139#143#diseaseC2699510 1172-1176 diseaseC2699510 denotes SHFM
11778160-8#139#143#diseaseC2699510 1172-1176 diseaseC2699510 denotes SHFM
11778160-8#168#172#gene344191 1201-1205 gene344191 denotes EVX2
100#104#gene323037#47#diseaseC0432028 11778160-7#100#104#gene3230 11778160-7#37#47#diseaseC0432028 associated_with HOXD,split foot
168#172#gene344191139#143#diseaseC2699510 11778160-8#168#172#gene344191 11778160-8#139#143#diseaseC2699510 associated_with EVX2,SHFM
168#172#gene344191139#143#diseaseC2699510 11778160-8#168#172#gene344191 11778160-8#139#143#diseaseC2699510 associated_with EVX2,SHFM
168#172#gene34419179#83#diseaseC2699510 11778160-8#168#172#gene344191 11778160-8#79#83#diseaseC2699510 associated_with EVX2,SHFM
168#172#gene34419179#83#diseaseC2699510 11778160-8#168#172#gene344191 11778160-8#79#83#diseaseC2699510 associated_with EVX2,SHFM
168#172#gene34419188#91#diseaseC2609259 11778160-8#168#172#gene344191 11778160-8#88#91#diseaseC2609259 associated_with EVX2,SPD
168#172#gene34419188#91#diseaseC2609259 11778160-8#168#172#gene344191 11778160-8#88#91#diseaseC2609259 associated_with EVX2,SPD
24#30#gene323962#79#diseaseC0206762 11778160-2#24#30#gene3239 11778160-2#62#79#diseaseC0206762 associated_with HOXD13,limb malformation
24#30#gene323996#99#diseaseC2609259 11778160-2#24#30#gene3239 11778160-2#96#99#diseaseC2609259 associated_with HOXD13,SPD
32#37#gene323561#75#diseaseC2699746 11778160-0#32#37#gene3235 11778160-0#61#75#diseaseC2699746 associated_with HOXD9,synpolydactyly
38#44#gene323961#75#diseaseC2699746 11778160-0#38#44#gene3239 11778160-0#61#75#diseaseC2699746 associated_with HOXD13,synpolydactyly
49#53#gene34419161#75#diseaseC2699746 11778160-0#49#53#gene344191 11778160-0#61#75#diseaseC2699746 associated_with EVX2,synpolydactyly
57#61#gene3230139#143#diseaseC2699510 11778160-8#57#61#gene3230 11778160-8#139#143#diseaseC2699510 associated_with HOXD,SHFM
57#61#gene3230139#143#diseaseC2699510 11778160-8#57#61#gene3230 11778160-8#139#143#diseaseC2699510 associated_with HOXD,SHFM
57#61#gene323079#83#diseaseC2699510 11778160-8#57#61#gene3230 11778160-8#79#83#diseaseC2699510 associated_with HOXD,SHFM
57#61#gene323079#83#diseaseC2699510 11778160-8#57#61#gene3230 11778160-8#79#83#diseaseC2699510 associated_with HOXD,SHFM
57#61#gene323088#91#diseaseC2609259 11778160-8#57#61#gene3230 11778160-8#88#91#diseaseC2609259 associated_with HOXD,SPD
57#61#gene323088#91#diseaseC2609259 11778160-8#57#61#gene3230 11778160-8#88#91#diseaseC2609259 associated_with HOXD,SPD