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- NCIT_C51234 IAO_0000115 "Human F7 wild-type allele is located within 13q34 and is approximately 14 kb in length. This allele, which encodes coagulation factor VII protein, plays a role in homeostasis and blood coagulation. Defects in the gene associated with variant alleles are causative agents for coagulopathy." @default.
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- NCIT_C51234 NCIT_P106 "Gene or Genome" @default.
- NCIT_C51234 NCIT_P108 "F7 wt Allele" @default.
- NCIT_C51234 NCIT_P207 "C1707994" @default.
- NCIT_C51234 NCIT_P211 "blood coagulation factor VII activity" @default.
- NCIT_C51234 NCIT_P211 "blood coagulation" @default.
- NCIT_C51234 NCIT_P211 "extracellular" @default.
- NCIT_C51234 NCIT_P211 "serine-type peptidase activity" @default.
- NCIT_C51234 NCIT_P321 "2155" @default.
- NCIT_C51234 NCIT_P366 "F7_wt_Allele" @default.
- NCIT_C51234 NCIT_P96 "Coagulation Factor VII" @default.
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- NCIT_C51234 hasExactSynonym "Coagulation Factor VII (Serum Prothrombin Conversion Accelerator) wt Allele" @default.
- NCIT_C51234 hasExactSynonym "F7 wt Allele" @default.
- NCIT_C51234 hasExactSynonym "FA7" @default.
- NCIT_C51234 hasExactSynonym "SPCA" @default.
- NCIT_C51234 type Class @default.
- NCIT_C51234 isDefinedBy ncit.owl @default.
- NCIT_C51234 label "F7 wt Allele" @default.
- NCIT_C51234 subClassOf NCIT_C16612 @default.
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