Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion type Assertion NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_head.
- NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion wasGeneratedBy ECO_0000203 NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_provenance.
- NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion wasDerivedFrom befree-2016 NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_provenance.
- NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion SIO_000772 20423741 NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_provenance.
- NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion evidence source_evidence_literature NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_provenance.
- NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_assertion description "[Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency (21-OHD) is an autosomal recessive disorder caused by the defective CYP21A2 gene that leads to various degrees of impaired secretion of both cortisol and aldosterone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808560.RABF6ZILMFPyrzABaoSWQjPylubuLyGGxYAe4LwLcYaW8130_provenance.