Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion> ?p ?o ?g. }
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- NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion type Assertion NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_head.
- NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion wasGeneratedBy ECO_0000203 NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_provenance.
- NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion wasDerivedFrom befree-20140225 NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_provenance.
- NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion SIO_000772 21689626 NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_provenance.
- NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion evidence source_evidence_literature NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_provenance.
- NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_assertion description "[Mutations in the human cadherin 23 (CDH23) gene cause deafness, neurosensory, autosomal recessive 12 (DFNB12) nonsyndromic hearing loss or Usher syndrome, type 1D (characterized by hearing impairment, vestibular dysfunction, and visual impairment).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478476.RAAAm7QxkK3qIERpDS2KwIpMTEhuZtxK4tvyISnCY9gkk130_provenance.