Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion description "[Mutations in the ATP-binding cassette transporter 1 (ABCA1) gene have been recently identified as the molecular defect in Tangier disease (TD) and familial high density lipoprotein deficiency (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion evidence source_evidence_literature NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion SIO_000772 11476965 NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion wasDerivedFrom befree-20140225 NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion wasGeneratedBy ECO_0000203 NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.