Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_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." NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_assertion evidence source_evidence_literature NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_assertion SIO_000772 12709788 NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_assertion wasDerivedFrom befree-20140225 NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_assertion wasGeneratedBy ECO_0000203 NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_provenance.