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SubjectPredicateObject
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Vallat J.-M."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Vallat J.-M."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Vandenberghe A."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Vandenberghe A."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Kassouri N."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Kassouri N."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Hammadouche T."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/author"Hammadouche T."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/date"2002"xsd:gYear
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/pages"726-736"xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/pages"726-736"xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/title"Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/title"Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse."xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/volume"70"xsd:string
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/volume"70"xsd:string
http://purl.uniprot.org/citations/11799477http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/11799477
http://purl.uniprot.org/citations/11799477http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/11799477
http://purl.uniprot.org/citations/11799477http://purl.uniprot.org/core/erratumhttp://purl.uniprot.org/citations/SIPFEBDD3CE23FBDBA8
http://purl.uniprot.org/uniprot/#_P02545-citation-11799477http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11799477
http://purl.uniprot.org/uniprot/#_P48678-citation-11799477http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11799477
http://purl.uniprot.org/uniprot/#_A0A384MQX1-mappedCitation-11799477http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11799477
http://purl.uniprot.org/uniprot/#_B4DFR3-mappedCitation-11799477http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11799477
http://purl.uniprot.org/uniprot/#_D3YUF7-mappedCitation-11799477http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11799477
http://purl.uniprot.org/uniprot/#_Q5TCI8-mappedCitation-11799477http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/11799477