Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP356435.RAbkCS3ftlyT2L5LpTO9sYqgDWZ-bs6HzV8pyT1wwa51U130_provenance.