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http://purl.uniprot.org/citations/10679252http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Awata T."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/pages"612-616"xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/name"Biochem. Biophys. Res. Commun."xsd:string
http://purl.uniprot.org/uniprot/O76024#attribution-2B7D1F853FC85A2362CCCD2CDD395360http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10679252
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/date"2000"xsd:gYear
http://purl.uniprot.org/uniprot/O76024http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/10679252
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/volume"268"xsd:string
http://purl.uniprot.org/citations/10679252http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10679252
http://purl.uniprot.org/citations/10679252http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10679252
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Katayama S."xsd:string
http://purl.uniprot.org/uniprot/#_O76024-citation-10679252http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10679252
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Ohkubo T."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.org/dc/terms/identifier"doi:10.1006/bbrc.2000.2169"xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Kurihara S."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Abe T."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Kanazawa Y."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/title"Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Takino H."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Inoue K."xsd:string
http://purl.uniprot.org/citations/10679252http://purl.uniprot.org/core/author"Inoue I."xsd:string