Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_assertion description "[Using expression microarrays and a unique method for comparative expression analysis called L2L, we sought to define this defect in cells lacking a functional CS group B (CSB) protein, the SWI/SNF-like ATPase responsible for most cases of CS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_assertion evidence source_evidence_literature NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_assertion SIO_000772 16772382 NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_assertion wasDerivedFrom befree-2016 NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_assertion wasGeneratedBy ECO_0000203 NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.
- befree-2016 importedOn "2016-02-19" NP554419.RAtI6-QYq-TqxSrNBrYGpVCn3gG75hgwV8b6WpTkMMY8M130_provenance.