Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion> ?p ?o ?g. }
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- NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion type Assertion NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_head.
- NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion description "[Mutant alleles of a third unconventional myosin, myosin XV, are associated with nonsyndromic, recessive, congenital deafness DFNB3 on human chromosome 17p11.2 and deafness in shaker2 (Myo15(sh2)) mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_provenance.
- NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion evidence source_evidence_literature NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_provenance.
- NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion SIO_000772 10704189 NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_provenance.
- NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion wasDerivedFrom befree-20150227 NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_provenance.
- NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_assertion wasGeneratedBy ECO_0000203 NP902765.RA-6dVr7pi61dzTKAL9AZLhv4sYF9JtM50_u6EBt_vhQY130_provenance.