Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion> ?p ?o ?g. }
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- NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion type Assertion NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_head.
- NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion wasGeneratedBy ECO_0000203 NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_provenance.
- NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion wasDerivedFrom befree-20150227 NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_provenance.
- NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion SIO_000772 21480433 NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_provenance.
- NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion evidence source_evidence_literature NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_provenance.
- NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_assertion description "[Although mutations in MYH14 have been shown to cause nonsyndromic autosomal dominant hearing loss (DFNA4), the peripheral neuropathy, myopathy, and hoarseness have not been associated with MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932549.RAUPXOykTg7nlb8LFiR4JvE5TmTlZSFpV_m9-VeRbn0lQ130_provenance.