Path ID: DB11608_MESH_D002836_1
Concepts
| Identifier | Name | Type |
|---|---|---|
| MESH:C000599709 | Eftrenonacog alfa | Disease |
| UniProt:P00740 | Coagulation factor IX | Protein |
| GO:0007597 | Blood coagulation, intrinsic pathway | BiologicalProcess |
| GO:0072378 | Blood coagulation, fibrin clot formation | BiologicalProcess |
| MESH:D002836 | Hereditary factor IX deficiency disease | Disease |
Relationships
NOTE: predicates are annotated in Biolink Model (v1.3.0)
| Subject | Predicate | Object |
|---|---|---|
| Eftrenonacog Alfa | CHEMICALLY SIMILAR TO | Coagulation Factor Ix |
| Coagulation Factor Ix | PARTICIPATES IN | Blood Coagulation, Intrinsic Pathway |
| Blood Coagulation, Intrinsic Pathway | POSITIVELY REGULATES | Blood Coagulation, Fibrin Clot Formation |
| Blood Coagulation, Fibrin Clot Formation | NEGATIVELY CORRELATED WITH | Hereditary Factor Ix Deficiency Disease |
Reference: