Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion type Assertion NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_head.
- NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_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." NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_provenance.
- NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion evidence source_evidence_literature NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_provenance.
- NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion SIO_000772 15734952 NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_provenance.
- NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion wasDerivedFrom befree-20140225 NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_provenance.
- NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_assertion wasGeneratedBy ECO_0000203 NP875193.RAZ84hEZrJrCe0JIjzzTEnHw7XAWNs_dflKbn1U-jiJ9E130_provenance.