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http://purl.uniprot.org/citations/10360404http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10360404http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10360404http://purl.org/dc/terms/identifier"doi:10.1002/(sici)1096-8628(19990611)84:5<484::aid-ajmg14>3.0.co;2-w"xsd:string
http://purl.uniprot.org/citations/10360404http://purl.org/dc/terms/identifier"doi:10.1002/(sici)1096-8628(19990611)84:5<484::aid-ajmg14>3.0.co;2-w"xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/author"Wong K."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/author"Wong K."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/author"Choy F.Y.M."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/author"Choy F.Y.M."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/author"Shi H.P."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/author"Shi H.P."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/name"Am. J. Med. Genet."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/name"Am. J. Med. Genet."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/pages"484-486"xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/pages"484-486"xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/title"Glucocerebrosidase mutations among Chinese neuronopathic and non-neuronopathic Gaucher disease patients."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/title"Glucocerebrosidase mutations among Chinese neuronopathic and non-neuronopathic Gaucher disease patients."xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/volume"84"xsd:string
http://purl.uniprot.org/citations/10360404http://purl.uniprot.org/core/volume"84"xsd:string
http://purl.uniprot.org/citations/10360404http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10360404
http://purl.uniprot.org/citations/10360404http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10360404
http://purl.uniprot.org/citations/10360404http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10360404
http://purl.uniprot.org/citations/10360404http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10360404
http://purl.uniprot.org/uniprot/P04062http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/10360404