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- NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_assertion type Assertion NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_head.
- NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_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." NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_provenance.
- NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_assertion evidence source_evidence_literature NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_provenance.
- NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_assertion SIO_000772 9580109 NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_provenance.
- NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_assertion wasDerivedFrom befree-2016 NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_provenance.
- NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_assertion wasGeneratedBy ECO_0000203 NP1394776.RAYnZhkKwBoFv0Cz8PpFzLgHF6NMYXUfHjGkR78G4zkLc130_provenance.