Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion> ?p ?o ?g. }
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- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion type Assertion NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_head.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion description "[Recent studies have implicated mutations in the ATP-binding cassette transporter A1, ABCA1, as a cause of Tangier disease (TD) and familial hypoalphalipoproteinemia (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion evidence source_evidence_literature NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion SIO_000772 14576201 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion wasDerivedFrom befree-2016 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.
- NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_assertion wasGeneratedBy ECO_0000203 NP418081.RAB76UVM1cfIZceaaVU5obIlCAtvkXmqn9WeNKl5c-yVM130_provenance.