Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_assertion description "[BRCA1 mutations are rare in sporadic cancers, but loss of BRCA1 resulting from reduced expression or incorrect subcellular localization is postulated to be important in non-familial breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_assertion evidence source_evidence_literature NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_assertion SIO_000772 9988281 NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_assertion wasDerivedFrom befree-2016 NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_assertion wasGeneratedBy ECO_0000203 NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1414759.RA96Z3Cr4DnDGFITW5d3AspBiDx8woztpd8WZ2GPBUuAM130_provenance.