Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion> ?p ?o ?g. }
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- NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion type Assertion NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_head.
- NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion wasGeneratedBy ECO_0000203 NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_provenance.
- NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion wasDerivedFrom befree-20140225 NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_provenance.
- NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion SIO_000772 16550584 NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_provenance.
- NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion evidence source_evidence_literature NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_provenance.
- NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_assertion description "[One of these genes, cadherin 23, produces a spectrum of phenotypic traits, including presbycusis, nonsyndromic prelingual hearing loss (DFNB12), and syndromic hearing loss as part of Usher syndrome (Usher 1D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP796034.RAE7co7Hm3Jf_PMWOTbFDi_4VKQxeA-SrU5bkcn280I-M130_provenance.