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http://purl.uniprot.org/uniprot/#_P00156-citation-11047755http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11047755
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/author"Anitori R."xsd:string
http://purl.uniprot.org/uniprot/P00156#attribution-310E40CF851420AA2B2DA58A20F9B555http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/11047755
http://purl.uniprot.org/citations/11047755http://purl.org/dc/terms/identifier"doi:10.1086/316900"xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/author"Keightley J.A."xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/name"Am. J. Hum. Genet."xsd:string
http://purl.uniprot.org/citations/11047755http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/11047755
http://purl.uniprot.org/citations/11047755http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11047755http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11047755
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/date"2000"xsd:gYear
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/author"Kennaway N.G."xsd:string
http://purl.uniprot.org/uniprot/P00156http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/11047755
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/author"Buist N.R.M."xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/volume"67"xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/author"Burton M.D."xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/pages"1400-1410"xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/author"Quan F."xsd:string
http://purl.uniprot.org/citations/11047755http://purl.uniprot.org/core/title"Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene."xsd:string
http://purl.uniprot.org/uniprot/#_Q9MJW3-citation-11047755http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11047755
http://purl.uniprot.org/uniprot/Q9MJW3http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/11047755