Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion type Assertion NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_head.
- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion description "[Congenital adrenal hyperplasia (CAH) due to steroid 21-hydroxylase deficiency is a common inherited disorder of adrenal hormone biosynthesis due to mutations in the 21-hydroxylase gene, CYP21A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_provenance.
- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion evidence source_evidence_literature NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_provenance.
- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion SIO_000772 19856253 NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_provenance.
- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion wasDerivedFrom befree-2016 NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_provenance.
- NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_assertion wasGeneratedBy ECO_0000203 NP771657.RACC_RD8sfMaUjqfVEAd_IyKdngc6StzkUjXMNur7tLZI130_provenance.