Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion> ?p ?o ?g. }
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- NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion type Assertion NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_head.
- NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion description "[Mutations in the 11beta-HSD2 gene cause a rare form of inherited hypertension, the syndrome of apparent mineralocorticoid excess (AME), in which cortisol activates the MR resulting in severe hypertension and hypokalemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion evidence source_evidence_literature NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion SIO_000772 16980198 NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion wasDerivedFrom befree-20150227 NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_assertion wasGeneratedBy ECO_0000203 NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.