Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_assertion> ?p ?o ?g. }
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- NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_assertion type Assertion NP279468.RAYUF-N1EjO81SHjPsYjCXwrCWzNmaLCp8GzIQxxKL-3w130_head.
- 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.