Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- befree-2016 importedOn "2016-02-19" NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_assertion wasGeneratedBy ECO_0000203 NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_assertion wasDerivedFrom befree-2016 NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_assertion SIO_000772 19744334 NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_assertion evidence source_evidence_literature NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.
- NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_assertion description "[The GJB2 gene accounted for the etiology in about 18.31% of the patients with hearing loss, SLC26A4 accounted for about 13.73%, and mtDNA 1555A>G mutation accounted for 1.76%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762470.RAf46smrgOTvMWuzFsOgHhMUwn24kOdRvy3t6XTUQe8jY130_provenance.