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- NCIT_C51235 IAO_0000115 "Human F8 wild-type allele is located within Xq28 and is approximately 548 kb in length. This allele, which encodes coagulation factor VIII protein, is involved in the intrinsic blood coagulation pathway. Defects in this gene generate variant alleles. These variants result in hemophilia A, a common recessive X-linked coagulation disorder." @default.
- NCIT_C51235 NCIT_NHC0 "C51235" @default.
- NCIT_C51235 NCIT_P100 "300841" @default.
- NCIT_C51235 NCIT_P102 "NM_000132" @default.
- NCIT_C51235 NCIT_P106 "Gene or Genome" @default.
- NCIT_C51235 NCIT_P107 "F8 wt Allele" @default.
- NCIT_C51235 NCIT_P108 "F8 wt Allele" @default.
- NCIT_C51235 NCIT_P207 "C1704822" @default.
- NCIT_C51235 NCIT_P211 "blood coagulation factor activity" @default.
- NCIT_C51235 NCIT_P211 "blood coagulation" @default.
- NCIT_C51235 NCIT_P321 "2157" @default.
- NCIT_C51235 NCIT_P322 "CTRP" @default.
- NCIT_C51235 NCIT_P366 "F8_wt_Allele" @default.
- NCIT_C51235 NCIT_P96 "Coagulation Factor VIII" @default.
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- NCIT_C51235 normalizedInformationContent "100" @default.
- NCIT_C51235 referenceCount "1" @default.
- NCIT_C51235 hasExactSynonym "AHF" @default.
- NCIT_C51235 hasExactSynonym "Coagulation Factor VIII, Procoagulant Component (Hemophilia A) wt Allele" @default.
- NCIT_C51235 hasExactSynonym "DXS1253E" @default.
- NCIT_C51235 hasExactSynonym "F8 wt Allele" @default.
- NCIT_C51235 hasExactSynonym "F8B" @default.
- NCIT_C51235 hasExactSynonym "F8C" @default.
- NCIT_C51235 hasExactSynonym "FVIII" @default.
- NCIT_C51235 hasExactSynonym "HEMA" @default.
- NCIT_C51235 inSubset NCIT_C116977 @default.
- NCIT_C51235 inSubset NCIT_C142799 @default.
- NCIT_C51235 inSubset NCIT_C142800 @default.
- NCIT_C51235 type Class @default.
- NCIT_C51235 isDefinedBy ncit.owl @default.
- NCIT_C51235 label "F8 wt Allele" @default.
- NCIT_C51235 subClassOf NCIT_C16612 @default.
- NCIT_C51235 subClassOf NCIT_C21295 @default.
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