Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_assertion description "[Mutations in the ATP-binding cassette transporter ABCA1 underlie Tangier disease and familial hypoalphaliproteinemia (FHA), disorders that are characterised by reduced high-density lipoprotein-cholesterol (HDL-C) concentration and cholesterol efflux, and increased coronary artery disease (CAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_assertion evidence source_evidence_literature NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_assertion SIO_000772 12709788 NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_assertion wasDerivedFrom befree-20140225 NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_assertion wasGeneratedBy ECO_0000203 NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP881778.RAFb0nyHV5rB-I-2pDVuu16Y-vA5LA4Oc2x-Zxw9skB9U130_provenance.