Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_assertion> ?p ?o ?g. }
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- NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_assertion type Assertion NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_head.
- NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_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." NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_provenance.
- NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_assertion evidence source_evidence_literature NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_provenance.
- NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_assertion SIO_000772 21480433 NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_provenance.
- NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_assertion wasDerivedFrom befree-20140225 NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_provenance.
- NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_assertion wasGeneratedBy ECO_0000203 NP264293.RATf1oct7Bqe5IqFETw9te7vDr77BHu2Z6KFlfyCTJGjI130_provenance.