Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_assertion description "[Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_assertion evidence source_evidence_curated NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_assertion SIO_000772 22405088 NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_assertion wasDerivedFrom uniprot-20150221 NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_assertion wasGeneratedBy ECO_0000218 NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4123.RAgVUiv6JPBfBgY_whQQibbm51WskwBQgzuQqJ0QiX0Xg130_provenance.