Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion type Assertion NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_head.
- NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_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." NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_provenance.
- NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion evidence source_evidence_literature NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_provenance.
- NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion SIO_000772 15639189 NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_provenance.
- NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion wasDerivedFrom befree-20150227 NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_provenance.
- NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_assertion wasGeneratedBy ECO_0000203 NP748902.RAs44rAFZrY8MA7XiM4eEjJYFHZ2MQUZNcZoqAqhfLpVQ130_provenance.