Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_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." NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_assertion evidence source_evidence_literature NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_assertion SIO_000772 12355548 NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_assertion wasDerivedFrom befree-20150227 NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_assertion wasGeneratedBy ECO_0000203 NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP342745.RAPCige5-5kpiwH5MrlGOW-cl3GPAg4W12NecDwVE_Wfc130_provenance.