Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_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." NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_assertion evidence source_evidence_literature NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_assertion SIO_000772 15734952 NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_assertion wasDerivedFrom befree-2016 NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_assertion wasGeneratedBy ECO_0000203 NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.
- befree-2016 importedOn "2016-02-19" NP482655.RATpZrkFWzyg6HyonFiZy68wj_AheDixML7RLv-4jjeso130_provenance.