Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_assertion> ?p ?o ?g. }
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- NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_assertion type Assertion NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_head.
- NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_assertion wasGeneratedBy ECO_0000203 NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_provenance.
- NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_assertion wasDerivedFrom befree-20140225 NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_provenance.
- NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_assertion SIO_000772 21480433 NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_provenance.
- NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_assertion evidence source_evidence_literature NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_provenance.
- NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_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." NP481498.RAd7N_AaCGYX9g5gIAu8v7znAYOLmilmeEk_rpk8o6AZo130_provenance.