Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion> ?p ?o ?g. }
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- NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion type Assertion NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_head.
- NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion description "[Most cases of congenital adrenal hyperplasia (CAH) are caused by mutations in this gene, and most mutations appear to arise from gene conversion-like events involving the transfer of deleterious sequences from the pseudogene, CYP21P, which is located within 30 kb of CYP21.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_provenance.
- NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion evidence source_evidence_literature NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_provenance.
- NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion SIO_000772 9836705 NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_provenance.
- NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion wasDerivedFrom befree-2016 NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_provenance.
- NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_assertion wasGeneratedBy ECO_0000203 NP1410074.RA32xN-8s7Zjn7HdNhOAPs6iIlgjHQ7tLacg7oVlVmOn0130_provenance.