Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion> ?p ?o ?g. }
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- NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_assertion type Assertion NP749888.RAgDlFBhL0_Au7ds9sSOUgZm3seDc877rF1IlZZ_ZcQac130_head.
- 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.