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http://purl.uniprot.org/diseases/439http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/439http://www.w3.org/2000/01/rdf-schema#comment"A severe form of Ehlers-Danlos syndrome, a group of connective tissue disorders characterized by skin hyperextensibility, articular hypermobility, and tissue fragility. EDSVASC is an autosomal dominant disease characterized by joint and dermal manifestations as in other forms of the syndrome, and by proneness to spontaneous rupture of bowel and large arteries. The vascular complications may affect all anatomical areas."xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/keywords/248
http://purl.uniprot.org/diseases/439http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/mim/130050
http://purl.uniprot.org/diseases/439http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://id.nlm.nih.gov/mesh/D004535
http://purl.uniprot.org/diseases/439http://www.w3.org/2000/01/rdf-schema#seeAlsohttp://purl.uniprot.org/medgen/C0268338
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#prefLabel"Ehlers-Danlos syndrome, vascular type"xsd:string
http://purl.uniprot.org/diseases/439http://purl.uniprot.org/core/mnemonic"EDSVASC"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"EDS IV"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"EDS4"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"Ehlers-Danlos syndrome 4"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"Ehlers-Danlos syndrome arterial type"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"Ehlers-Danlos syndrome ecchymotic type"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"Sack-Barabas syndrome"xsd:string
http://purl.uniprot.org/diseases/439http://www.w3.org/2004/02/skos/core#altLabel"Ehlers-Danlos syndrome, type IV, autosomal dominant"xsd:string
http://purl.uniprot.org/uniprot/P02461#SIP9255637E1324E2F7http://purl.uniprot.org/core/diseasehttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001768http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001769http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001770http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001771http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001772http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001773http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001774http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001777http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439
http://purl.uniprot.org/annotation/VAR_001779http://www.w3.org/2004/02/skos/core#relatedhttp://purl.uniprot.org/diseases/439