Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_assertion> ?p ?o ?g. }
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- NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_assertion type Assertion NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_head.
- NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_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." NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_provenance.
- NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_assertion evidence source_evidence_literature NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_provenance.
- NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_assertion SIO_000772 17223983 NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_provenance.
- NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_assertion wasDerivedFrom befree-20150227 NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_provenance.
- NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_assertion wasGeneratedBy ECO_0000203 NP800087.RAU1pgOjLuS3WZpmyc1vSdqNVEbkKwGAxc9wkkxw7-MLM130_provenance.