Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion type Assertion NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_head.
- NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion description "[The chimeric CYP21P/CYP21 gene is a consequence of a 26- or 32-kb deletion in the C4-CYP21 repeat module of CYP21P, tenascin A ( XA), serine/threonine nuclear protein kinase ( RP2), and the C4B and CYP21 genes in congenital adrenal hyperplasia (CAH) with steroid 21-hydroxylase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_provenance.
- NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion evidence source_evidence_literature NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_provenance.
- NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion SIO_000772 14730433 NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_provenance.
- NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion wasDerivedFrom befree-2016 NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_provenance.
- NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_assertion wasGeneratedBy ECO_0000203 NP428533.RAAeTnKKVXYCqNb5cj3xEtiT16EIYwrdzm4HzDrIGcFws130_provenance.