Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_assertion> ?p ?o ?g. }
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- NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_assertion type Assertion NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_head.
- NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_assertion wasGeneratedBy ECO_0000203 NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_provenance.
- NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_assertion wasDerivedFrom befree-20140225 NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_provenance.
- NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_assertion SIO_000772 17466001 NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_provenance.
- NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_assertion evidence source_evidence_literature NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_provenance.
- NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_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." NP798757.RAwoJLAK4TppwAkFPwL7hq5ylXJAO6SP7eF1gebC1KtfQ130_provenance.