Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_assertion description "[Recently, mutations in the electron donor enzyme P450 oxidoreductase were identified as the cause of CAH with apparent combined 17alpha-hydroxylase and 21-hydroxylase deficiency, thereby illustrating the impact of redox regulation enzymes on steroidogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_assertion evidence source_evidence_literature NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_assertion SIO_000772 17223983 NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_assertion wasDerivedFrom befree-20140225 NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_assertion wasGeneratedBy ECO_0000203 NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP514012.RAnZEogabB0QP5FqaAqGH2F-uv8Dcf8HO9WtLlfbg1WTY130_provenance.