Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion type Assertion NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_head.
- NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion description "[Peroxisomal acyl-coenzyme A (acyl-CoA) oxidase deficiency is an autosomal recessive inborn error of peroxisomal fatty acid oxidation due to a deficiency of straight-chain acyl-CoA oxidase (SCOX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_provenance.
- NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion evidence source_evidence_literature NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_provenance.
- NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion SIO_000772 17458872 NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_provenance.
- NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion wasDerivedFrom befree-20150227 NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_provenance.
- NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_assertion wasGeneratedBy ECO_0000203 NP220800.RATuqp2gQrDumdo1BvysCLXP9R3W9xl-rGEVloGCtUioY130_provenance.