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- source_evidence_literature type ECO_0000212 NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion description "[Mutations in the gene (GJB2) coding for Connexin 26 (Cx26) are responsible for genetic forms of sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion evidence source_evidence_literature NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion SIO_000772 15996214 NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion wasDerivedFrom befree-2016 NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion wasGeneratedBy ECO_0000203 NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_provenance.