Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_assertion> ?p ?o ?g. }
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- NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_assertion type Assertion NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_head.
- NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_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." NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_provenance.
- NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_assertion evidence source_evidence_curated NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_provenance.
- NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_assertion SIO_000772 14576201 NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_provenance.
- NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_assertion wasDerivedFrom uniprot-2016 NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_provenance.
- NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_assertion wasGeneratedBy ECO_0000218 NP3066.RAKMaeAz17miiuUpjadv8Fj9rQNICGyUaNgE6hM-FdEfc130_provenance.