Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion> ?p ?o ?g. }
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- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion type Assertion NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_head.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion description "[Neonatal screening for steroid 21-hydroxylase (CYP21) deficiency is performed to identify congenital adrenal hyperplasia (CAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion evidence source_evidence_literature NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion SIO_000772 15608154 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion wasDerivedFrom befree-2016 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.
- NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_assertion wasGeneratedBy ECO_0000203 NP473362.RACqnZgebkhQOPdMsYofKsUQLwEAoWqHz_fEo4nt4d-a8130_provenance.