Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion> ?p ?o ?g. }
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- NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion type Assertion NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_head.
- NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion description "[Mutations in the kidney isozyme of human 11-hydroxysteroid dehydrogenase (11-HSD2) cause apparent mineralocorticoid excess, an autosomal recessive form of familial hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_provenance.
- NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion evidence source_evidence_literature NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_provenance.
- NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion SIO_000772 10523339 NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_provenance.
- NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion wasDerivedFrom befree-20140225 NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_provenance.
- NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_assertion wasGeneratedBy ECO_0000203 NP857547.RAaNxbswYf5BSosHy3q1-6-aJvLDNS1fwJUa3lnlq8LgY130_provenance.