Matches in Nanopublications for { ?s ?p "[Spinocerebellar ataxia type 14 (SCA14) is an autosomal-dominant ataxia caused by point mutations of the Protein Kinase C Gamma gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP642882.RAdZI3Uc3n69zFe7sXCqn2v43M9QT9yCHUQAzmTE0iU6k130_assertion description "[Spinocerebellar ataxia type 14 (SCA14) is an autosomal-dominant ataxia caused by point mutations of the Protein Kinase C Gamma gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642882.RAdZI3Uc3n69zFe7sXCqn2v43M9QT9yCHUQAzmTE0iU6k130_provenance.
- assertion description "[Spinocerebellar ataxia type 14 (SCA14) is an autosomal-dominant ataxia caused by point mutations of the Protein Kinase C Gamma gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1110071.RAA4RUkfVUhrLFDHmsTgimMOi99Ixi7c65NZolPK87LUA130_assertion description "[Spinocerebellar ataxia type 14 (SCA14) is an autosomal-dominant ataxia caused by point mutations of the Protein Kinase C Gamma gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1110071.RAA4RUkfVUhrLFDHmsTgimMOi99Ixi7c65NZolPK87LUA130_provenance.