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PubMed:6086495 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T1 20-45 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T2 146-171 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T3 173-176 DiseaseOrPhenotypicFeature denotes BMD D020388
T4 329-332 DiseaseOrPhenotypicFeature denotes BMD D020388

Test-merged

Id Subject Object Predicate Lexical cue #label
T4 329-332 DiseaseOrPhenotypicFeature denotes BMD D020388
T3 173-176 DiseaseOrPhenotypicFeature denotes BMD D020388
T2 146-171 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T1 20-45 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T18559 717-729 GeneOrGeneProduct denotes X chromosome
T77304 373-385 GeneOrGeneProduct denotes X chromosome
T9868 229-241 GeneOrGeneProduct denotes X chromosome
T89063 75-87 GeneOrGeneProduct denotes X chromosome

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T1 75-87 GeneOrGeneProduct denotes X chromosome
T2 229-241 GeneOrGeneProduct denotes X chromosome
T3 373-385 GeneOrGeneProduct denotes X chromosome
T4 717-729 GeneOrGeneProduct denotes X chromosome

Test-merged-2

Id Subject Object Predicate Lexical cue #label
T89063 75-87 GeneOrGeneProduct denotes X chromosome
T9868 229-241 GeneOrGeneProduct denotes X chromosome
T77304 373-385 GeneOrGeneProduct denotes X chromosome
T18559 717-729 GeneOrGeneProduct denotes X chromosome
T1 20-45 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T2 146-171 DiseaseOrPhenotypicFeature denotes Becker muscular dystrophy D020388
T3 173-176 DiseaseOrPhenotypicFeature denotes BMD D020388
T4 329-332 DiseaseOrPhenotypicFeature denotes BMD D020388

DisGeNET

Id Subject Object Predicate Lexical cue
T0 329-332 gene:1756 denotes BMD
T1 146-171 disease:C0917713 denotes Becker muscular dystrophy
T2 329-332 gene:7439 denotes BMD
T3 146-171 disease:C0917713 denotes Becker muscular dystrophy
R1 T0 T1 associated_with BMD,Becker muscular dystrophy
R2 T2 T3 associated_with BMD,Becker muscular dystrophy

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 20-45 Modifier:C537666 denotes Becker muscular dystrophy
T2 146-171 SpecificDisease:C537666 denotes Becker muscular dystrophy
T3 173-176 SpecificDisease:C537666 denotes BMD
T4 329-332 Modifier:C537666 denotes BMD
T5 420-451 CompositeMention:D020388|C537666 denotes Becker and Duchenne dystrophies