Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_assertion description "[Carriers of heterozygous mutations in BRCA1 or BRCA2 are strongly predisposed to breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_assertion evidence source_evidence_literature NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_assertion SIO_000772 15955736 NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_assertion wasDerivedFrom befree-2016 NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_assertion wasGeneratedBy ECO_0000203 NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.
- befree-2016 importedOn "2016-02-19" NP499412.RAVvJJFnxKoo3D8LgW35AD_UJ7x64TnZrXud63ARV791A130_provenance.