Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_assertion wasGeneratedBy ECO_0000203 NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_assertion wasDerivedFrom gad-20150221 NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_assertion SIO_000772 19027966 NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_assertion evidence source_evidence_literature NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.
- NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_assertion description "[Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134638.RAHw7BFE6O_MNAvOClQX8jFcgwmuq-r2UBcFaA1tfplWc130_provenance.