Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion> ?p ?o ?g. }
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- NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion type Assertion NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_head.
- NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion wasGeneratedBy ECO_0000203 NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_provenance.
- NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion wasDerivedFrom befree-2016 NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_provenance.
- NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion SIO_000772 19931309 NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_provenance.
- NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion evidence source_evidence_literature NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_provenance.
- NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_assertion description "[This would be similar to the clinical findings in familial glucocorticoid deficiency type 1, an autosomal recessive condition due to inactivating mutations of the adrenal receptor for ACTH, also known as the melanocortin 2 receptor (MC2R).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP777143.RAlDbqKzbCwLi-2hCcwNC_Ok5rdVQzfjMqqBroZTjdKU0130_provenance.