Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion> ?p ?o ?g. }
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- NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion type Assertion NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_head.
- NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion description "[The largest homozygous region (~11 Mb) in the affected family members was mapped to chromosome 9, which harbors deafness, autosomal recessive 31 (DFNB31; a gene previously associated with Usher syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_provenance.
- NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion evidence source_evidence_literature NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_provenance.
- NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion SIO_000772 21738389 NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_provenance.
- NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion wasDerivedFrom befree-2016 NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_provenance.
- NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_assertion wasGeneratedBy ECO_0000203 NP907959.RAALszXxt-z5nfxYLBT_HTDiX0PU7BYEQMCHRc6qLGags130_provenance.