Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion> ?p ?o ?g. }
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- NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion type Assertion NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_head.
- NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_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." NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_provenance.
- NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion evidence source_evidence_literature NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_provenance.
- NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion SIO_000772 15639189 NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_provenance.
- NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion wasDerivedFrom befree-2016 NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_provenance.
- NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_assertion wasGeneratedBy ECO_0000203 NP475366.RAxNx-ryGMJMzSRlo3IKx-5Va1o4BoQeGK5ryOwiJ9hvA130_provenance.