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- NCIT_C51237 IAO_0000115 "Human VWF wild-type allele is located in the vicinity of 12p13.31 and is approximately 176 kb in length. This allele, which encodes von Willebrand factor protein, plays a role in factor transport, platelet-vessel wall mediation, and coagulation. Mutations in this gene or deficiencies in this protein result in von Willebrand disease." @default.
- NCIT_C51237 NCIT_NHC0 "C51237" @default.
- NCIT_C51237 NCIT_P100 "613160" @default.
- NCIT_C51237 NCIT_P102 "NM_000552" @default.
- NCIT_C51237 NCIT_P106 "Gene or Genome" @default.
- NCIT_C51237 NCIT_P107 "VWF wt Allele" @default.
- NCIT_C51237 NCIT_P108 "VWF wt Allele" @default.
- NCIT_C51237 NCIT_P207 "C1710605" @default.
- NCIT_C51237 NCIT_P211 "binding" @default.
- NCIT_C51237 NCIT_P211 "blood coagulation" @default.
- NCIT_C51237 NCIT_P211 "cell adhesion" @default.
- NCIT_C51237 NCIT_P211 "extracellular space" @default.
- NCIT_C51237 NCIT_P211 "hemostasis" @default.
- NCIT_C51237 NCIT_P211 "secretory vesicle" @default.
- NCIT_C51237 NCIT_P321 "7450" @default.
- NCIT_C51237 NCIT_P322 "CTRP" @default.
- NCIT_C51237 NCIT_P366 "VWF_wt_Allele" @default.
- NCIT_C51237 NCIT_P96 "von Willebrand Factor" @default.
- NCIT_C51237 NCIT_R130 NCIT_C17132 @default.
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- NCIT_C51237 NCIT_R175 NCIT_C26323 @default.
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- NCIT_C51237 NCIT_R40 NCIT_C12219 @default.
- NCIT_C51237 NCIT_R40 NCIT_C13282 @default.
- NCIT_C51237 NCIT_R40 NCIT_C13377 @default.
- NCIT_C51237 NCIT_R40 NCIT_C13432 @default.
- NCIT_C51237 NCIT_R40 NCIT_C13446 @default.
- NCIT_C51237 NCIT_R40 NCIT_C14135 @default.
- NCIT_C51237 NCIT_R40 NCIT_C32221 @default.
- NCIT_C51237 NCIT_R40 NCIT_C34070 @default.
- NCIT_C51237 NCIT_R40 NCIT_C81849 @default.
- NCIT_C51237 NCIT_R41 NCIT_C14182 @default.
- NCIT_C51237 NCIT_R41 NCIT_C14225 @default.
- NCIT_C51237 NCIT_R41 NCIT_C14234 @default.
- NCIT_C51237 NCIT_R41 NCIT_C14250 @default.
- NCIT_C51237 NCIT_R41 NCIT_C14262 @default.
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- NCIT_C51237 NCIT_R41 NCIT_C25796 @default.
- NCIT_C51237 NCIT_R41 NCIT_C79740 @default.
- NCIT_C51237 normalizedInformationContent "100" @default.
- NCIT_C51237 referenceCount "1" @default.
- NCIT_C51237 hasExactSynonym "F8VWF" @default.
- NCIT_C51237 hasExactSynonym "FVIII-VWF" @default.
- NCIT_C51237 hasExactSynonym "VWD" @default.
- NCIT_C51237 hasExactSynonym "VWF wt Allele" @default.
- NCIT_C51237 hasExactSynonym "Von Willebrand Factor wt Allele" @default.
- NCIT_C51237 hasExactSynonym "von Willebrand Disease Gene" @default.
- NCIT_C51237 inSubset NCIT_C116977 @default.
- NCIT_C51237 inSubset NCIT_C142799 @default.
- NCIT_C51237 inSubset NCIT_C142800 @default.
- NCIT_C51237 type Class @default.
- NCIT_C51237 isDefinedBy ncit.owl @default.
- NCIT_C51237 label "VWF wt Allele" @default.
- NCIT_C51237 subClassOf NCIT_C16612 @default.
- NCIT_C51237 subClassOf NCIT_C21295 @default.
- NCIT_C51237 subClassOf NCIT_C28480 @default.
- NCIT_C51237 subClassOf NCIT_C28483 @default.
- NCIT_C51237 subClassOf NCIT_C51237 @default.
- NCIT_C51237 equivalentClass B23a2ec79d5d7a7cae1d0268888de9e81 @default.
- NCIT_C51237 equivalentClass B3b5ad88b9fdd434f1fd60ed6c3b37aee @default.