Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_assertion description "[In men with low HDL-C and CHD: 1) the LPL N9 and S291 alleles are more frequent than in CHD-free men with normal HDL-C, whereas the X447 allele is less frequent, and 2) the LPL N9 allele is associated with the LDL subclass response to gemfibrozil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_assertion evidence source_evidence_literature NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_assertion SIO_000772 15292370 NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_assertion wasDerivedFrom befree-2016 NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_assertion wasGeneratedBy ECO_0000203 NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.
- befree-2016 importedOn "2016-02-19" NP454616.RAQpYSs7MtUStsqrDruFcH6k5rAiv73enng67ZBhdUb_0130_provenance.