Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion> ?p ?o ?g. }
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- NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion type Assertion NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_head.
- NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion description "[Important advances made in the past year have included identification of KCNJ5 potassium channel mutations in the pathogenesis of both aldosterone-producing adenomas and familial hyperaldosteronism type III; characterization of phosphodiesterase 11A as a modifier of phenotype in Carney complex caused by protein kinase, cAMP-dependent, regulatory subunit, type-I mutations; the finding of 11?-hydroxysteroid dehydrogenase type I mutations as a novel mechanism for cortisone reductase deficiency; and demonstration of potential mortality benefit in pursuing comprehensive presymptomatic screening for patients with Li-Fraumeni syndrome, including possible reduction in risks associated with adrenocortical carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_provenance.
- NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion evidence source_evidence_literature NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_provenance.
- NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion SIO_000772 22476103 NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_provenance.
- NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion wasDerivedFrom befree-20150227 NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_provenance.
- NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_assertion wasGeneratedBy ECO_0000203 NP899087.RAjho--1eLONc8wFDauxOsNNIwsEfsd-ByfXgc35R0jXo130_provenance.