Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_assertion> ?p ?o ?g. }
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- NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_assertion type Assertion NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_head.
- NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_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." NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_provenance.
- NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_assertion evidence source_evidence_literature NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_provenance.
- NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_assertion SIO_000772 17223983 NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_provenance.
- NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_assertion wasDerivedFrom befree-20140225 NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_provenance.
- NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_assertion wasGeneratedBy ECO_0000203 NP394188.RA6MRxg1fNeuWYHPbuRS1jIXSa9wTYOAusXqK1Q9EM5sA130_provenance.