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http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"van Goor H."xsd:string
http://purl.uniprot.org/citations/9618173http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/9618173http://purl.org/dc/terms/identifier"doi:10.1093/hmg/7.7.1143"xsd:string
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/pages"1143-1148"xsd:string
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"Uitto J."xsd:string
http://purl.uniprot.org/uniprot/#_P04259-citation-9618173http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/9618173
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/date"1998"xsd:gYear
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"Smith F.J.D."xsd:string
http://purl.uniprot.org/uniprot/P04259#attribution-683A86C71EC62BBAE29559833C8B83F8http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/9618173
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"Covello S.P."xsd:string
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"Coleman C.M."xsd:string
http://purl.uniprot.org/citations/9618173http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/9618173
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/volume"7"xsd:string
http://purl.uniprot.org/uniprot/P04259#attribution-36B97F46D636AB14C53E96538967A1CAhttp://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/9618173
http://purl.uniprot.org/citations/9618173http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/9618173
http://purl.uniprot.org/uniprot/P04259http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/9618173
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/name"Hum. Mol. Genet."xsd:string
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/title"A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2."xsd:string
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"McLean W.H.I."xsd:string
http://purl.uniprot.org/citations/9618173http://purl.uniprot.org/core/author"Jonkman M.F."xsd:string