Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion type Assertion NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_head.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion description "[Mutations generating inactive enzymes have been described in the HSD11B2 gene in the congenital syndrome of apparent mineralocorticoid excess (AME)--a low renin form of hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_provenance.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion evidence source_evidence_literature NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_provenance.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion SIO_000772 9247735 NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_provenance.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion wasDerivedFrom befree-20150227 NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_provenance.
- NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_assertion wasGeneratedBy ECO_0000203 NP466061.RA4b4zWgADzYU8fd8qCIoOM30aaTTqTAdd4VAuR-ENBlk130_provenance.