RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Taylor L."xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Howell N."xsd:string
http://purl.uniprot.org/citations/1928099http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/1928099http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/1928099
http://purl.uniprot.org/citations/1928099http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/1928099
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/name"Am. J. Hum. Genet."xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/volume"49"xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Turnbull D.M."xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"McCullough D.A."xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/pages"939-950"xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/date"1991"xsd:gYear
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Mackey D."xsd:string
http://purl.uniprot.org/uniprot/#_P03886-citation-1928099http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/1928099
http://purl.uniprot.org/uniprot/P03886#attribution-03BB2582E4260F348A9660F8DF2B9471http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/1928099
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Poulton J."xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Kubacka I."xsd:string
http://purl.uniprot.org/uniprot/P03886http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/1928099
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/title"Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees."xsd:string
http://purl.uniprot.org/citations/1928099http://purl.uniprot.org/core/author"Bindoff L.A."xsd:string