Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_assertion> ?p ?o ?g. }
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- NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_assertion type Assertion NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_head.
- NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_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." NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_assertion evidence source_evidence_literature NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_assertion SIO_000772 17458872 NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_assertion wasDerivedFrom befree-20140225 NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_assertion wasGeneratedBy ECO_0000203 NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.