Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion> ?p ?o ?g. }
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- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion type Assertion NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_head.
- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_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." NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_provenance.
- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion evidence source_evidence_literature NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_provenance.
- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion SIO_000772 9247735 NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_provenance.
- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion wasDerivedFrom befree-20140225 NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_provenance.
- NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_assertion wasGeneratedBy ECO_0000203 NP501379.RAExx4Tx3oymoT_okScn0yN6KnJOoVpmT9weOYKSPD9ac130_provenance.