Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion> ?p ?o ?g. }
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- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion type Assertion NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_head.
- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion description "[We have shown that Tangier disease, a rare and severe form of HDL deficiency characterised by a biochemical defect in cellular cholesterol efflux, is caused by mutations in the ATP-binding-cassette (ABC1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_provenance.
- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion evidence source_evidence_literature NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_provenance.
- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion SIO_000772 10533863 NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_provenance.
- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion wasDerivedFrom befree-20140225 NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_provenance.
- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion wasGeneratedBy ECO_0000203 NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_provenance.