Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_assertion type Assertion NP502342.RAD0GJAACYjdENJ7pImHPrty7KQ5pGHW_AW58s5LRWlOQ130_head.
- 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.