Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP273179.RARO_GbMemU5XhvsS280WJDfxNUS9xbo-ez4-BVjAaMI4#assertion> ?p ?o ?g. }
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- assertion description "[In addition, the haplotype of CYP21 with chimera CYP21P/CYP21 causes 21-hydroxylase deficiency in congenital adrenal hyperplasia (CAH), while chimera TNXA/TNXB is associated with Ehlers-Danols syndrome as well as CAH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion evidence source_evidence_literature provenance.
- assertion SIO_000772 15639189 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion wasGeneratedBy ECO_0000203 provenance.