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- source_evidence_literature type ECO_0000212 NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_assertion description "[Branchio-oto-renal syndrome (BOR) is an autosomal dominant developmental disorder characterized by the association of branchial arch defects, hearing loss, and renal anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_assertion evidence source_evidence_literature NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_assertion SIO_000772 17357085 NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_assertion wasDerivedFrom befree-20140225 NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_assertion wasGeneratedBy ECO_0000203 NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP558029.RAiWWw_65qh3jAiHo6ubAOTOo3EFDrJYl8DuCyfOzItnU130_provenance.