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http://purl.uniprot.org/keywords/852http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Concept
http://purl.uniprot.org/keywords/852http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/94
http://purl.uniprot.org/keywords/852http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/356
http://purl.uniprot.org/keywords/852http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/core/Concept
http://purl.uniprot.org/keywords/852http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/9995
http://purl.uniprot.org/keywords/852http://www.w3.org/2000/01/rdf-schema#subClassOfhttp://purl.uniprot.org/keywords/9999
http://purl.uniprot.org/keywords/852http://www.w3.org/2000/01/rdf-schema#comment"Protein which, if defective, causes von Willebrand disease, a hemorrhagic disorder in which the von Willebrand factor is either quantitatively or qualitatively abnormal. Usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII and impaired platelet adhesion."xsd:string
http://purl.uniprot.org/keywords/852http://www.w3.org/2004/02/skos/core#prefLabel"von Willebrand disease"xsd:string
http://purl.uniprot.org/keywords/852http://purl.uniprot.org/core/categoryhttp://purl.uniprot.org/keywords/9995
http://purl.uniprot.org/uniprot/P07359http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/852
http://purl.uniprot.org/uniprot/P04275http://purl.uniprot.org/core/classifiedWithhttp://purl.uniprot.org/keywords/852
http://purl.uniprot.org/keywords/94http://www.w3.org/2004/02/skos/core#narrowerhttp://purl.uniprot.org/keywords/852
http://purl.uniprot.org/keywords/9995http://www.w3.org/2004/02/skos/core#narrowerhttp://purl.uniprot.org/keywords/852