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http://purl.uniprot.org/citations/23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/23871123http://www.w3.org/2000/01/rdf-schema#comment"To investigate the role of mutations in the sphingomyelin phosphodiesterase (SMPD1) gene in Parkinson's disease (PD) we sequenced all the exons of this gene in 198 Chinese PD cases and matched healthy control subjects. We identified 4 rare variants in SMPD1 (p.P332R, p.Y500H, p.P533L, and p.R591C) that were present only in cases and not in control subjects. Interestingly, 2 of these variants were previously reported in Chinese Niemann-Pick disease patients. Next, we genotyped these variants in another 806 PD cases and 7481 control subjects. We identified a novel, rare SMPD1 variant (p.R591C) which increased the risk of PD (p = 0.009)."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.org/dc/terms/identifier"doi:10.1016/j.neurobiolaging.2013.06.010"xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Liu J."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Tan E.K."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Foo J.N."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Liany H."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Tan L.C."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Bei J.X."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Yu X.Q."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Au W.L."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/author"Prakash K.M."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/name"Neurobiol Aging"xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/pages"2890.e13-5"xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/title"Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease."xsd:string
http://purl.uniprot.org/citations/23871123http://purl.uniprot.org/core/volume"34"xsd:string
http://purl.uniprot.org/citations/23871123http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/23871123
http://purl.uniprot.org/citations/23871123http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/23871123
http://purl.uniprot.org/uniprot/#_Q15496-mappedCitation-23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871123
http://purl.uniprot.org/uniprot/#_E9LUE6-mappedCitation-23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871123
http://purl.uniprot.org/uniprot/#_E9LUE7-mappedCitation-23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871123
http://purl.uniprot.org/uniprot/#_E9LUE8-mappedCitation-23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871123
http://purl.uniprot.org/uniprot/#_E9LUE9-mappedCitation-23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871123
http://purl.uniprot.org/uniprot/#_G3V1E1-mappedCitation-23871123http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/23871123