von Willebrand Disease, Type 1

Download in:

Switch to

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	umls-semnetwork:T047, skos:Concept
calbc:hasCorrelation	calbc-group:ANAT, calbc-group:CHEM, calbc-group:CONC, calbc-group:DISO, calbc-group:PHEN, calbc-group:PROC
skos:exactMatch	pubmed-mesh:von Willebrand Disease, Type 1
skos:definition	MSH: A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
skos:inScheme	lld:umls
skos-xl:prefLabel	umls-label:A17012079
skos-xl:altLabel	umls-label:A18433056, umls-label:A19288875, umls-label:A19288882, umls-label:A19295667, umls-label:A19295668, umls-label:A19291298, umls-label:A18440127, umls-label:A17012080, umls-label:A18437776, umls-label:A17003889, umls-label:A19293031, umls-label:A18435392, umls-label:A16995563, umls-label:A18444954, umls-label:A19293032, umls-label:A19294689