Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_assertion description "[Subjects with the variant genotypes for SNPs in four of the seven genes evaluated had small increases in bladder cancer risk compared to subjects with the homozygous wild-type genotypes: RAD23B IVS5-15A>G (OR, 1.3; 95% CI, 1.1-1.5; P = 0.01), ERCC2 R156R (OR, 1.3; 95% CI, 1.1-1.6; P = 0.006), ERCC1 IVS5+33A>C (OR, 1.2; 95% CI, 1.0-1.5; P = 0.06; P(trend) = 0.04), and ERCC5 M254V (OR, 1.4; 95% CI, 1.0-2.0; P = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_assertion evidence source_evidence_literature NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_assertion SIO_000772 16537713 NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_assertion wasDerivedFrom befree-20150227 NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_assertion wasGeneratedBy ECO_0000203 NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663478.RARsdrjJhC9bB89DA_C6fbfWi7uaxBl803_mZicIYKHsU130_provenance.