Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_assertion description "[Linkage and sequence mutation analyses of the ADOA candidate genes OPA1, OPA3, OPA4, and OPA5, including the genes WFS1, GJB2, and GJB6 associated with recessive inherited OA or dominant LFSNHL, were performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_assertion evidence source_evidence_literature NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_assertion SIO_000772 16648378 NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_assertion wasDerivedFrom befree-20140225 NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_assertion wasGeneratedBy ECO_0000203 NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.
- befree-20140225 importedOn "2014-02-25" NP399932.RAe2XeXDSyKhEgGWijS35Ks-hmD5fqaFNa18lo3Q_D884130_provenance.