Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_assertion> ?p ?o ?g. }
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- NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_assertion type Assertion NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_head.
- NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_assertion wasGeneratedBy ECO_0000203 NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_provenance.
- NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_assertion wasDerivedFrom befree-20140225 NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_provenance.
- NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_assertion SIO_000772 21480433 NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_provenance.
- NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_assertion evidence source_evidence_literature NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_provenance.
- NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_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." NP377462.RApzLqX88amhO6B2EYz6VMxcTLz_5NKvstgS3K_398GGQ130_provenance.