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- NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_assertion type Assertion NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_head.
- NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_assertion wasGeneratedBy ECO_0000203 NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_provenance.
- NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_assertion wasDerivedFrom befree-2016 NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_provenance.
- NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_assertion SIO_000772 21689626 NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_provenance.
- NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_assertion evidence source_evidence_literature NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_provenance.
- NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_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." NP903537.RAqmTBjWnUTA251mb3P-eeBQLGuawf9AwfBpFibn6UoIY130_provenance.