Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion description "[A cohort of 1,575 BRCA1 and 856 BRCA2 mutation carriers was used to evaluate haplotypes at ATM, BARD1, BRIP1, CTIP, MRE11, NBS1, RAD50, RAD51, and TOPBP1 in ovarian cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion evidence source_evidence_literature NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion SIO_000772 19584272 NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion wasDerivedFrom befree-2016 NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion wasGeneratedBy ECO_0000203 NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.
- befree-2016 importedOn "2016-02-19" NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_provenance.