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GENE - TERM ANNOTATION REPORT

RGD ID: 13959257
Species: Sus scrofa
RGD Object: Gene
Symbol: F11
Name: coagulation factor XI
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
F11 ISOF11 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:10593931 PMID:15026311 PMID:15140127 PMID:16835901 PMID:2052060 PMID:23929304 PMID:24033266 PMID:25741868 PMID:2813350 PMID:28492532 PMID:31064749 PMID:9326232
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