Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_assertion description "[Mutations in the Connexin 26 (Cx26) gene have been found to account for approximately 20% of all childhood deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_assertion evidence source_evidence_literature NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_assertion SIO_000772 12121355 NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_assertion wasDerivedFrom befree-20140225 NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_assertion wasGeneratedBy ECO_0000203 NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173948.RA4xd7v2KUzfWV8c4iuQXvCS1DjeJC6bY5_DwLRMwoOQg130_provenance.