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http://purl.uniprot.org/citations/2071611http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/name"J. Biol. Chem."xsd:string
http://purl.uniprot.org/uniprot/P02679#attribution-65364221A159923F90204DB8211CF7CChttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/2071611
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/author"Koopman J."xsd:string
http://purl.uniprot.org/uniprot/#_P02679-citation-2071611http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/2071611
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/author"Lord S.T."xsd:string
http://purl.uniprot.org/citations/2071611http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/2071611
http://purl.uniprot.org/citations/2071611http://purl.org/dc/terms/identifier"doi:10.1016/s0021-9258(18)98861-7"xsd:string
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/author"Briet E."xsd:string
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/pages"13456-13461"xsd:string
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/date"1991"xsd:gYear
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/title"A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization."xsd:string
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/author"Haverkate F."xsd:string
http://purl.uniprot.org/citations/2071611http://purl.uniprot.org/core/volume"266"xsd:string
http://purl.uniprot.org/uniprot/P02679http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/2071611
http://purl.uniprot.org/citations/2071611http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/2071611