Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP927017.RAg4tIEJR3n-H0n-CMYirWXdEcxGHsVjVk8pTkq_qH-Nc#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion wasGeneratedBy ECO_0000218 provenance.
- assertion wasDerivedFrom CTD_human provenance.
- assertion SIO_000772 18398334 provenance.
- assertion evidence source_evidence_curated provenance.
- assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.