Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion> ?p ?o ?g. }
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- NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion type Assertion NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_head.
- NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion description "[Steroid 21-hydroxylase deficiency is the underlying cause in over 90% of patients with congenital adrenal hyperplasia, an inherited metabolic disorder of adrenal steroidogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_provenance.
- NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion evidence source_evidence_literature NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_provenance.
- NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion SIO_000772 9580109 NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_provenance.
- NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion wasDerivedFrom befree-2016 NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_provenance.
- NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_assertion wasGeneratedBy ECO_0000203 NP1394777.RAIC8_aufNMJIg5HC3DfuBrhKZM8eoodpRIJ_o8_JRc9E130_provenance.