Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- befree-20150227 importedOn "2015-02-27" NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_assertion wasGeneratedBy ECO_0000203 NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_assertion wasDerivedFrom befree-20150227 NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_assertion SIO_000772 17272748 NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_assertion evidence source_evidence_literature NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.
- NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_assertion description "[High frequency of a retinoid X receptor gamma gene variant in familial combined hyperlipidemia that associates with atherogenic dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676827.RA4N7QUhzy09cOGlGn-XsfoVPcWAds0ZcXKWR1m9irz10130_provenance.