Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion> ?p ?o ?g. }
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- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion type Assertion NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_head.
- 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.