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An Entity of Type : owl:Axiom, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Axiom
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
Type	http://purl.obolibrary.org/obo/ECO_0007636 http://purl.obolibrary.org/obo/ECO_0007637
annotatedProperty	http://purl.obolibrary.org/obo/IAO_0000115
annotatedSource	factor XIII deficiency
annotatedTarget	A blood coagulation disease that is characterized by easy bleeding, has_symptom prolonged umbilical cord bleeding, epistaxis, bleeding of the gums, menorrhagia, recurrent miscarriages, abnormal scar formation and wound healing, and hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation of the F13A1 or F13B gene, which encodes Factor XIII, formally known as fibrin stabilizing factor.
database_cross_reference	url:https://ghr.nlm.nih.gov/condition/factor-xiii-deficiency#inheritance url:http://omim.org/entry/613225 url:http://omim.org/entry/613235
is topic of	Human Disease Ontology

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