Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_assertion description "[Despite extensive analysis of the BRCA1 and BRCA2 genes, germline mutations are detected in <20% of families with a presumed genetic predisposition for breast and ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_assertion evidence source_evidence_literature NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_assertion SIO_000772 22370629 NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_assertion wasDerivedFrom befree-2016 NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_assertion wasGeneratedBy ECO_0000203 NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.
- befree-2016 importedOn "2016-02-19" NP963816.RAVo6A39VPUSFLqP4zIWgSl18Ur84SOJ4fqFS2cLl28oI130_provenance.