Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion> ?p ?o ?g. }
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- NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion type Assertion NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_head.
- NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion wasGeneratedBy ECO_0000203 NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_provenance.
- NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion wasDerivedFrom befree-20150227 NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_provenance.
- NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion SIO_000772 17466001 NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_provenance.
- NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion evidence source_evidence_literature NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_provenance.
- NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_assertion description "[Patients lacked mutations in other genes known to cause ACTH resistance, including AAAS for patients diagnosed with triple A syndrome and MC2R and MRAP for patients diagnosed with familial glucocorticoid deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540231.RAW0J-d6Y0EN-mXygx5QSPsCMuGwK3JxAkp-53YqG8iZE130_provenance.