Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_assertion wasGeneratedBy ECO_0000203 NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_assertion wasDerivedFrom befree-2016 NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_assertion SIO_000772 21366435 NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_assertion evidence source_evidence_literature NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.
- NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_assertion description "[We also used this approach to scan for mutations in KCNJ10 and FOXI1, two genes reported to play a role in the pathogenesis of Pendred syndrome and enlarged vestibular aqueduct.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876554.RAsPDM3W8HGDo_hxO_oihKlPr9X2CrXUhHysIpS4vVcZQ130_provenance.