Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_assertion description "[To evaluate contribution of single nucleotide polymorphisms (SNPs) of X-ray repair cross-complementing group 1 (XRCC1) gene to the risk of cervical carcinoma, we conducted a case-control study of 1012 patients including 539 carcinoma and 473 cervical intraepithelial neoplasia (CIN) and 800 normal women controls and genotyped three XRCC1 SNPs (Arg194Trp, Arg280His, and Arg399Gln).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_assertion evidence source_evidence_literature NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_assertion SIO_000772 17504380 NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_assertion wasDerivedFrom befree-20150227 NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_assertion wasGeneratedBy ECO_0000203 NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779983.RAt7mVCb3SZxlxiSiBgU7FlyQLxALU5vShLlWt8wTOCXQ130_provenance.