Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion type Assertion NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_head.
- NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion description "[Although there was little statistical power to detect modest increases in risk for the homozygote variant genotypes, particularly for the rare RAD51 and XRCC2 variants, the data suggest that none of these variants play a major role in the etiology of breast or ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_provenance.
- NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion evidence source_evidence_literature NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_provenance.
- NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion SIO_000772 15734952 NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_provenance.
- NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion wasDerivedFrom befree-2016 NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_provenance.
- NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_assertion wasGeneratedBy ECO_0000203 NP482664.RAvmheSY_rh5Xx5W4ughRKojkyKwbIKsG8g0RIXneZD3s130_provenance.