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PubMed:11778160 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 61-75 DiseaseOrPhenotypicFeature denotes synpolydactyly 0000722|0019683|0021651
T4 282-296 DiseaseOrPhenotypicFeature denotes synpolydactyly 0000722|0019683|0021651
T7 298-301 DiseaseOrPhenotypicFeature denotes SPD 0019683|0000722
T9 573-601 DiseaseOrPhenotypicFeature denotes split-hand/foot malformation 0016576
T10 603-607 DiseaseOrPhenotypicFeature denotes SHFM 0016576
T11 675-678 DiseaseOrPhenotypicFeature denotes SPD 0019683|0000722
T13 907-917 DiseaseOrPhenotypicFeature denotes split foot 0017450
T14 1112-1116 DiseaseOrPhenotypicFeature denotes SHFM 0016576
T15 1121-1124 DiseaseOrPhenotypicFeature denotes SPD 0019683|0000722
T17 1172-1176 DiseaseOrPhenotypicFeature denotes SHFM 0016576

FSU-PRGE

Id Subject Object Predicate Lexical cue
T1 32-37 protein denotes HOXD9
T2 38-44 protein denotes HOXD13
T3 49-53 protein denotes EVX2
T4 127-131 protein denotes HoxD
T5 226-232 protein denotes HOXD13
T6 334-338 protein denotes HOXD
T7 494-498 protein denotes HOXD
T8 733-737 protein denotes HOXD
T9 847-852 protein denotes HOXD9
T10 853-859 protein denotes HOXD13
T11 864-868 protein denotes EVX2
T12 970-974 protein denotes HOXD
T13 1090-1094 protein denotes HOXD
T14 1201-1205 protein denotes EVX2
T15 1287-1291 protein denotes HOXD

PIR-corpus2

Id Subject Object Predicate Lexical cue
T1 32-37 protein denotes HOXD9
T2 38-44 protein denotes HOXD13
T3 49-53 protein denotes EVX2
T4 127-131 protein denotes HoxD
T5 226-232 protein denotes HOXD13
T6 334-338 protein denotes HOXD
T7 494-498 protein denotes HOXD
T8 733-737 protein denotes HOXD
T9 847-852 protein denotes HOXD9
T10 853-859 protein denotes HOXD13
T11 864-868 protein denotes EVX2
T12 970-974 protein denotes HOXD
T13 1090-1094 protein denotes HOXD
T14 1201-1205 protein denotes EVX2
T15 1210-1216 protein denotes D2S294
T16 1287-1291 protein denotes HOXD

DisGeNET5_gene_disease

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#100#104#gene3230 970-974 gene3230 denotes HOXD
11778160-7#37#47#diseaseC0432028 907-917 diseaseC0432028 denotes split foot
11778160-8#57#61#gene3230 1090-1094 gene3230 denotes HOXD
11778160-8#168#172#gene344191 1201-1205 gene344191 denotes EVX2
11778160-8#79#83#diseaseC2699510 1112-1116 diseaseC2699510 denotes SHFM
11778160-8#88#91#diseaseC2609259 1121-1124 diseaseC2609259 denotes SPD
11778160-8#139#143#diseaseC2699510 1172-1176 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#139#143#diseaseC2699510 1172-1176 diseaseC2699510 denotes SHFM
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
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
100#104#gene323037#47#diseaseC0432028 11778160-7#100#104#gene3230 11778160-7#37#47#diseaseC0432028 associated_with HOXD,split foot
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#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#gene323088#91#diseaseC2609259 11778160-8#57#61#gene3230 11778160-8#88#91#diseaseC2609259 associated_with HOXD,SPD
57#61#gene3230139#143#diseaseC2699510 11778160-8#57#61#gene3230 11778160-8#139#143#diseaseC2699510 associated_with HOXD,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#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#gene34419188#91#diseaseC2609259 11778160-8#168#172#gene344191 11778160-8#88#91#diseaseC2609259 associated_with EVX2,SPD
168#172#gene344191139#143#diseaseC2699510 11778160-8#168#172#gene344191 11778160-8#139#143#diseaseC2699510 associated_with EVX2,SHFM

DisGeNET

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