Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_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." NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance.