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http://purl.uniprot.org/uniprot/P02545http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/citations/10080180http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/10080180
http://purl.uniprot.org/uniprot/P02545#attribution-36CAD9DB98D6DEF71C79F9BBB5CF27DChttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/pages"285-288"xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/volume"21"xsd:string
http://purl.uniprot.org/citations/10080180http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/10080180
http://purl.uniprot.org/uniprot/P02545#attribution-1D4D8DB59D2CC1D332ACB2A7913B078Ehttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Di Barletta M.R."xsd:string
http://purl.uniprot.org/uniprot/P02545#attribution-6FB53938263C2A4DE10EB0B50537F75Fhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/uniprot/P02545#attribution-E4D18D815E146F6D4779AE4A54518FCFhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/name"Nat. Genet."xsd:string
http://purl.uniprot.org/uniprot/#_P02545-citation-10080180http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Hammouda E.-H."xsd:string
http://purl.uniprot.org/uniprot/P02545#attribution-2164712EFAC0D9B6ADD9EB86396BA621http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/10080180
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Merlini L."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Varnous S."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/title"Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.org/dc/terms/identifier"doi:10.1038/6799"xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Becane H.-M."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Muntoni F."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Duboc D."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Urtizberea J.-A."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Greenberg C.R."xsd:string
http://purl.uniprot.org/citations/10080180http://purl.uniprot.org/core/author"Bonne G."xsd:string