Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_assertion description "[Furthermore, the combined genotypes GSTM1 null/ CYP2E1(*)5B, GSTM1 null/mEH YY, and GSTT1 null/mEH YY are significantly associated with susceptibility to AR (OR = 15.42, 95% CI = 1.33-77.93, P = 0.021; OR = 3.48, 95% CI = 1.63-8.04, P = 0.0008; OR = 3.4; 95% CI = 0.99-17.38, P = 0.05; respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_assertion evidence source_evidence_literature NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_assertion SIO_000772 12355548 NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_assertion wasDerivedFrom gad-20150221 NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_assertion wasGeneratedBy ECO_0000203 NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76403.RAiZsPv6ooB05IIZ-_iFSBRNh3aUtcjwMkEL9-InOW9aQ130_provenance.