Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- 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.
- ctd_human-20130708 importedOn "2013-07-24" NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.