DESCRIBE <http://purl.uniprot.org/diseases/1744>

Subject	Predicate	Object
http://purl.uniprot.org/diseases/1744	http://www.w3.org/1999/02/22-rdf-syntax-ns#type	http://purl.uniprot.org/core/Disease
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#comment	"Autosomal recessive coagulation defect. Patients with HWMK deficiency do not have a hemorrhagic tendency, but they exhibit abnormal surface-mediated activation of fibrinolysis."xsd:string
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#seeAlso	http://purl.uniprot.org/mim/228960
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#seeAlso	http://purl.uniprot.org/medgen/C0272340
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#seeAlso	http://purl.uniprot.org/medgen/C1856719
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#seeAlso	http://purl.uniprot.org/medgen/C2673570
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#seeAlso	http://purl.uniprot.org/medgen/C2673571
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2000/01/rdf-schema#seeAlso	http://purl.uniprot.org/medgen/C2673572
http://purl.uniprot.org/diseases/1744	http://www.w3.org/2004/02/skos/core#prefLabel	"High molecular weight kininogen deficiency"xsd:string
http://purl.uniprot.org/diseases/1744	http://purl.uniprot.org/core/mnemonic	"HMWK deficiency"xsd:string
http://purl.uniprot.org/uniprot/P01042#SIP2830AC73CDF40992	http://purl.uniprot.org/core/disease	http://purl.uniprot.org/diseases/1744