Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_assertion description "[High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_assertion evidence source_evidence_literature NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_assertion SIO_000772 23643325 NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_assertion wasDerivedFrom befree-20140225 NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_assertion wasGeneratedBy ECO_0000203 NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP734214.RA1B4RiJcyY9qOtDigYY2mzKLJg4j8IJSeaefD3pkn4-s130_provenance.