Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_assertion> ?p ?o ?g. }
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- NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_assertion type Assertion NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_head.
- NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_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." NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_provenance.
- NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_assertion evidence source_evidence_literature NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_provenance.
- NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_assertion SIO_000772 10704189 NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_provenance.
- NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_assertion wasDerivedFrom befree-20140225 NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_provenance.
- NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_assertion wasGeneratedBy ECO_0000203 NP892000.RAV2IoUkRNPIK8namY9ZBHP6mGfuwdLihDoE2Vlj4a2xw130_provenance.