Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion> ?p ?o ?g. }
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- NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion type Assertion NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_head.
- NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion description "[Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_provenance.
- NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion evidence source_evidence_literature NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_provenance.
- NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion SIO_000772 15996214 NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_provenance.
- NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion wasDerivedFrom befree-2016 NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_provenance.
- NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_assertion wasGeneratedBy ECO_0000203 NP502341.RAgvTqAX53X7YRnP79eCkL2g2XIMBzHz7G5WD4A2qUpe8130_provenance.