Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion> ?p ?o ?g. }
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- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion type Assertion NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_head.
- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion wasGeneratedBy ECO_0000218 NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion wasDerivedFrom ctd_human-20130708 NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion SIO_000772 18398334 NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion evidence source_evidence_curated NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_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." NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.