Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_assertion description "[Mutations in the two known major breast cancer susceptibility genes, BRCA1 and BRCA2, account for a minority of familial breast cancer, whereas families without mutations in these genes (BRCAX group) account for 70% of familial breast cancer cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_assertion evidence source_evidence_literature NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_assertion SIO_000772 18094411 NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_assertion wasDerivedFrom befree-20140225 NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_assertion wasGeneratedBy ECO_0000203 NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP245963.RAwxpN3YwBsVpH5AR007p3nYiJqm1qs3o1HSWiRM87fJ0130_provenance.