Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_assertion> ?p ?o ?g. }
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- NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_assertion type Assertion NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_head.
- NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_assertion wasGeneratedBy ECO_0000203 NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_provenance.
- NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_assertion wasDerivedFrom befree-20150227 NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_provenance.
- NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_assertion SIO_000772 21480433 NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_provenance.
- NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_assertion evidence source_evidence_literature NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_provenance.
- NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_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." NP932551.RAWLw8ueHg2p1sM28-Xl2vwWaSGzO04u3bKCRmjCi0M50130_provenance.