Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion type Assertion NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_head.
- NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_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." NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_provenance.
- NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion evidence source_evidence_literature NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_provenance.
- NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion SIO_000772 15639189 NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_provenance.
- NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion wasDerivedFrom befree-20150227 NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_provenance.
- NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_assertion wasGeneratedBy ECO_0000203 NP748857.RA4BIz_YpcvuEkeL63JM_XV6t_a_w8aPpKM8VCe0EPLjI130_provenance.