Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion> ?p ?o ?g. }
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- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion type Assertion NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_head.
- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_provenance.
- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion evidence source_evidence_curated NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_provenance.
- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion SIO_000772 21480433 NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_provenance.
- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion wasDerivedFrom uniprot-20130724 NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_provenance.
- NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_assertion wasGeneratedBy ECO_0000218 NP4277.RAqy3nfDiIvy2hYiiEAbWxDHPE5dYWtA20NJkrHvKhzpY130_provenance.