Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion> ?p ?o ?g. }
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- NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion type Assertion NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_head.
- 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.
- NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion evidence source_evidence_literature NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance.
- NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion SIO_000772 19931309 NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance.
- NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion wasDerivedFrom befree-20150227 NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance.
- NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_assertion wasGeneratedBy ECO_0000203 NP548281.RA--NlKwGPB5XTLtesjZLh2IZdl_3z0yKwq4xzPUhIhBQ130_provenance.