Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_assertion description "[We used the allelic discrimination method to identify polymorphisms in GSTT1, SULT1C2, CDA, SXR (drug metabolic pathways), XPD, XPA, XPG, ERCC1, TOP2A (DNA repair), VEGF (angiogenesis), and MDR1 (multidrug resistance) genes in 110 adult patients with intermediate-risk AML, enrolled in the CETLAM-99 prospective trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_assertion evidence source_evidence_literature NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_assertion SIO_000772 16507781 NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_assertion wasDerivedFrom befree-2016 NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_assertion wasGeneratedBy ECO_0000203 NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.
- befree-2016 importedOn "2016-02-19" NP538059.RAYPiuEI7Na8LbI4BHAThP7DC2P557aGwqlOYDoI-g9Co130_provenance.