Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_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." NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_assertion evidence source_evidence_literature NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_assertion SIO_000772 16537713 NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_assertion wasDerivedFrom gad-20150221 NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_assertion wasGeneratedBy ECO_0000203 NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.
- gad-20150221 importedOn "2015-02-21" NP53725.RAEmfiiB3sS7S5Z445O-v3tx49rcSAq104H-c4J0TBc_Y130_provenance.