Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion type Assertion NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_head.
- NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion description "[Tangier disease (TD) is a rare autosomal recessive disease characterized by plasma high-density lipoprotein deficiency caused by an ATP-binding cassette transporter A1 ( ABCA1) gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_provenance.
- NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion evidence source_evidence_literature NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_provenance.
- NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion SIO_000772 12111381 NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_provenance.
- NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion wasDerivedFrom befree-20140225 NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_provenance.
- NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_assertion wasGeneratedBy ECO_0000203 NP792670.RA0WuijGdmSzevcMV9pAoT-aQesrHQywMornnV_JZA74k130_provenance.