Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP559838.RAxn1CpwCAcxn17t2aP4iGJuxKQDXpJjWzrIb4R95OAeo130_provenance.