Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_assertion description "[We identified genetic variants in TPMT (rs12201199, P value = 0.00022, OR = 17.0, 95% CI 2.3-125.9) and COMT (rs9332377, P value = 0.00018, OR = 5.5, 95% CI 1.9-15.9) associated with cisplatin-induced hearing loss in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_assertion evidence source_evidence_literature NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_assertion SIO_000772 19898482 NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_assertion wasDerivedFrom befree-20140225 NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_assertion wasGeneratedBy ECO_0000203 NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP781597.RAhtIDVcZKA7rvEP0VUAj33yScIYbgT6nZVjGcfpHTbX8130_provenance.