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PubMed:15122708 / 818-839 JSONTXT

Annnotations TAB JSON ListView MergeView

TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T10 0-21 DiseaseOrPhenotypicFeature denotes multiminicore disease C564969

Test-merged-2

Id Subject Object Predicate Lexical cue #label
T10 0-21 DiseaseOrPhenotypicFeature denotes multiminicore disease C564969

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15122708-4#261#282#diseaseC0270962 0-21 diseaseC0270962 denotes multiminicore disease
15122708-4#261#282#diseaseC1850674 0-21 diseaseC1850674 denotes multiminicore disease
15122708-4#261#282#diseaseC0270962 0-21 diseaseC0270962 denotes multiminicore disease
15122708-4#261#282#diseaseC1850674 0-21 diseaseC1850674 denotes multiminicore disease