Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_assertion description "[We believe that given the growing appreciation of the prognostic significance of BRCA mutations and the differential chemosensitivity shown by these tumors, as well as the potential of novel agents such as poly(ADP-ribose) polymerase inhibitors, the identification of a germline BRCA mutation concurrent with a new diagnosis of ovarian cancer will significantly impact on tailoring personalized ovarian management in the future.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_assertion evidence source_evidence_literature NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_assertion SIO_000772 20973257 NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_assertion wasDerivedFrom befree-2016 NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_assertion wasGeneratedBy ECO_0000203 NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP847829.RAUlb2uU5iYs3iEqIGUYdkBRRFnCpODFaKyfWkstQsGwQ130_provenance.