Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_assertion description "[Identification of mutations in the ATP binding cassette transporter 1 (ABCA1) gene in patients with Tangier disease, who exhibit reduced HDL cholesterol and apolipoprotein A1 concentrations and premature coronary atherosclerosis, has led us to hypothesise that ABCA1 could play a key role in the onset of premature CHD in FH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_assertion evidence source_evidence_literature NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_assertion SIO_000772 12624133 NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_assertion wasDerivedFrom befree-20150227 NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_assertion wasGeneratedBy ECO_0000203 NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP218606.RAV5RaFVxGdWgRp6PK72sPnrlHlJWqsw4RlJzEQfpz4SY130_provenance.