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http://purl.uniprot.org/citations/11058897http://purl.org/dc/terms/identifier"doi:10.1002/1098-1004(200011)16:5<401::aid-humu4>3.0.co;2-j"xsd:string
http://purl.uniprot.org/citations/11058897http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/11058897
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/pages"401-407"xsd:string
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/author"Longo N."xsd:string
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/title"Functional analysis of mutations in the OCTN2 transporter causing primary carnitine deficiency: lack of genotype-phenotype correlation."xsd:string
http://purl.uniprot.org/uniprot/O76082http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/11058897
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/volume"16"xsd:string
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/author"Taroni F."xsd:string
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/author"Garavaglia B."xsd:string
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/11058897http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/11058897
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/date"2000"xsd:gYear
http://purl.uniprot.org/citations/11058897http://purl.uniprot.org/core/name"Hum. Mutat."xsd:string
http://purl.uniprot.org/uniprot/O76082#attribution-7F55319FE28D4637E8B4E5F3B906E8DChttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/11058897
http://purl.uniprot.org/citations/11058897http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/uniprot/#_O76082-citation-11058897http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11058897