Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_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." NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_assertion evidence source_evidence_curated NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_assertion SIO_000772 16949155 NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_assertion wasDerivedFrom ctd_human-20150221 NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_assertion wasGeneratedBy ECO_0000218 NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP24430.RAchKAaF9XJZtTY2sE12mwXQpwxEHPeIuNNQJj9fm41X0130_provenance.