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SubjectPredicateObject
http://purl.uniprot.org/citations/17412732http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17412732
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"DiMauro S."xsd:string
http://purl.uniprot.org/uniprot/Q547S8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/uniprot/#_A0A3G6ZET5-mappedCitation-17412732http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/uniprot/#_B4DEQ0-mappedCitation-17412732http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/uniprot/Q16134#attribution-36D24C890F7E2A263267718AFDD1F00Fhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/citations/17412732http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17412732
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Lochmueller H."xsd:string
http://purl.uniprot.org/uniprot/#_Q547S8-mappedCitation-17412732http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/name"Brain"xsd:string
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Naini A."xsd:string
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Talim B."xsd:string
http://purl.uniprot.org/citations/17412732http://purl.org/dc/terms/identifier"doi:10.1093/brain/awm054"xsd:string
http://purl.uniprot.org/uniprot/A7UNU5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Hirano M."xsd:string
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/volume"130"xsd:string
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/title"The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene."xsd:string
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Gempel K."xsd:string
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/uniprot/A0A2I6U1Q3http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/uniprot/Q16134#attribution-1F8FCCBA919206698B6F9862FDA350A3http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Kale G."xsd:string
http://purl.uniprot.org/uniprot/A0A3G6ZET5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/17412732
http://purl.uniprot.org/citations/17412732http://purl.uniprot.org/core/author"Quinzii C."xsd:string
http://purl.uniprot.org/uniprot/#_Q16134-citation-17412732http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/17412732