Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_assertion description "[The IVS-178G>A SNP in COX10 and the c+1120C>T SNP in COX15 were significantly less represented in the patient group (P < 0.001 and P = 0.017, respectively) with respective odd ratios of 0.22 and 0.59, suggesting a possible protective role toward the risk for AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_assertion evidence source_evidence_literature NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_assertion SIO_000772 19826901 NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_assertion wasDerivedFrom befree-20140225 NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_assertion wasGeneratedBy ECO_0000203 NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP297854.RAQsSTNvbjutyiQ4nSiQ2lhgIp0JcdmcXXt8h0PDCBDyA130_provenance.