Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_assertion> ?p ?o ?g. }
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- NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_assertion type Assertion NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_head.
- NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_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." NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_provenance.
- NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_assertion evidence source_evidence_literature NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_provenance.
- NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_assertion SIO_000772 17223983 NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_provenance.
- NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_assertion wasDerivedFrom befree-2016 NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_provenance.
- NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_assertion wasGeneratedBy ECO_0000203 NP588859.RAYeWSUxZ4HE5TNRpE_bFUMV2nEY9nUhprHXlbZS1UYbI130_provenance.