Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- befree-2016 importedOn "2016-02-19" NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_assertion wasGeneratedBy ECO_0000203 NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_assertion wasDerivedFrom befree-2016 NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_assertion SIO_000772 21689626 NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_assertion evidence source_evidence_literature NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.
- NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_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." NP903536.RAJewdRHsuVur05S6UBqRqiaE32J-dL7LGMUa1jFLZGTk130_provenance.