Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_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." NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_assertion evidence source_evidence_literature NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_assertion SIO_000772 17223983 NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_assertion wasDerivedFrom befree-2016 NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_assertion wasGeneratedBy ECO_0000203 NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.
- befree-2016 importedOn "2016-02-19" NP588863.RAjHsJQnsCc11BQhhCt0CJlmuKOO5vK20VP2GNQMpfB3g130_provenance.