Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_assertion description "[These results suggest that the different types of Cx26 mutations affect autosomal recessive NSHL according to ethnic background.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_assertion evidence source_evidence_literature NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_assertion SIO_000772 10983956 NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_assertion wasDerivedFrom gad-20150221 NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_assertion wasGeneratedBy ECO_0000203 NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP51539.RAQ3dkaVtCbmYrXHmjxC2KwDfLsp_I8UMq6x0EWdPoFqI130_provenance.