Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_assertion description "[We tested 303 unrelated Czech patients with early hearing loss (298 with NSHL and 5 with PS), all GJB2-negative, for SLC26A4 mutations and evaluated their clinical and radiological phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_assertion evidence source_evidence_literature NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_assertion SIO_000772 20597900 NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_assertion wasDerivedFrom befree-20140225 NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_assertion wasGeneratedBy ECO_0000203 NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP533318.RAvJD3hOHHeKWs6_17xN1zRo5qz7m0893TFeNFkdEJJdA130_provenance.