Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_assertion description "[For UADT cancer risk, associations were observed for the homozygous carriers of the variant alleles of MGMT L84F [odds ratio (OR) 2.35, 95% confidence interval (CI) 1.32-4.20], MGMT 171C > T (OR 2.24, 95% CI 1.20-4.17) and OGG1 S326C (OR 2.07, 95% CI 1.15-3.73) whilst three variants were associated with a protective effect (XPA 23G > A, P for trend 0.022, APEX Q51H, P for trend 0.036, CHEK2 intron 9-200T > C, P for trend 0.009).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_assertion evidence source_evidence_literature NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_assertion SIO_000772 17040931 NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_assertion wasDerivedFrom befree-20150227 NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_assertion wasGeneratedBy ECO_0000203 NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP779093.RASADUwVK68OsFQ3MqyhBPHcb_8u9bQTP0w9uKrZACIBU130_provenance.