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http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/author"Brooks S.S."xsd:string
http://purl.uniprot.org/uniprot/P10253#attribution-E0DF7E0B3EBCA924F3D0D82C08512F9Chttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/7981676
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/author"Hirschhorn R."xsd:string
http://purl.uniprot.org/citations/7981676http://purl.org/dc/terms/identifier"doi:10.1093/hmg/3.7.1081"xsd:string
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/name"Hum. Mol. Genet."xsd:string
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/author"Huie M.L."xsd:string
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/title"A de novo 13 nt deletion, a newly identified C647W missense mutation and a deletion of exon 18 in infantile onset glycogen storage disease type II (GSDII)."xsd:string
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/uniprot/#_P10253-citation-7981676http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7981676
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/author"Grix A."xsd:string
http://purl.uniprot.org/citations/7981676http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7981676http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7981676
http://purl.uniprot.org/uniprot/P10253http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/7981676
http://purl.uniprot.org/citations/7981676http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7981676
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/pages"1081-1087"xsd:string
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/author"Chen A.S."xsd:string
http://purl.uniprot.org/citations/7981676http://purl.uniprot.org/core/volume"3"xsd:string