Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_assertion description "[Furthermore, the greater risk for the double variant of p53 and XRCC1 in the SOD2 Val/Val genotype group was specific only for patients with adenocarcinoma and not for patients with squamous cell carcinoma, with adjusted ORs of 3.31 (95% CI, 1.68-6.51) and 0.69 (95% CI, 0.24-2.02), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_assertion evidence source_evidence_literature NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_assertion SIO_000772 15534883 NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_assertion wasDerivedFrom befree-20140225 NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_assertion wasGeneratedBy ECO_0000203 NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP346850.RA2OpO18XHT5D2mfYzuGlnWovMb-_1T_LNbdmgkj7JW1s130_provenance.