Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_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." NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_assertion evidence source_evidence_literature NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_assertion SIO_000772 17458872 NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_assertion wasDerivedFrom befree-2016 NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_assertion wasGeneratedBy ECO_0000203 NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.
- befree-2016 importedOn "2016-02-19" NP606450.RAe6mu_RWgdm40DnS_p0YNR7_0PyYH6T_bklX_r649lQI130_provenance.