Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_assertion description "[Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_assertion evidence source_evidence_literature NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_assertion SIO_000772 10533863 NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_assertion wasDerivedFrom befree-20150227 NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_assertion wasGeneratedBy ECO_0000203 NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936325.RARrn2TYkcam7jiQM1uIgiLNPWWB9M1fz8mVh0YHS9JeA130_provenance.