Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_assertion description "[Two polymorphic sites of the microsomal epoxide hydrolase gene (EPHX1, 113Tyr-->113His, 139His-->139Arg) and four glutathione S-transferase genes (GSTM1, GSTM3, GSTP1, GSTT1) were genotyped in a group of patients with larynx cancer (N=204) and in a group of healthy controls (N=203), all Spanish caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_assertion evidence source_evidence_literature NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_assertion SIO_000772 12359356 NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_assertion wasDerivedFrom befree-20140225 NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_assertion wasGeneratedBy ECO_0000203 NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP203971.RAEISQy4vmDa5SFvzXE6D_-tmPUvWOdRVTA2FLuVWBFw0130_provenance.