Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_assertion description "[Individuals who carried polymorphisms for GSTT1 null and/or high activity microsomal epoxide hydrolase (mEH 113YY+139HR or 113YY+139RR or 113YH+139RR) and/or low activity NAD(P)H:quinone oxidoreductase 1 (NQO1 187PS/SS) were 1.65, 2.49 and 13 times more likely to have MM (P(trend)=0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_assertion evidence source_evidence_literature NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_assertion SIO_000772 16949155 NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_assertion wasDerivedFrom befree-20140225 NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_assertion wasGeneratedBy ECO_0000203 NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP815485.RA6Syt031mCWV4gFkyzkTrRcHBK6U_WbYrfMU1gHwnIXU130_provenance.