diff --git a/src/ontology/mondo-edit.obo b/src/ontology/mondo-edit.obo
index 4bae718bf..91fda9ea9 100644
--- a/src/ontology/mondo-edit.obo
+++ b/src/ontology/mondo-edit.obo
@@ -135982,7 +135982,7 @@ xref: SCTID:286951002 {source="DOID:10824"}
 xref: SCTID:70272006 {source="EFO:1001031", source="MONDO:equivalentTo", source="DOID:10824"}
 xref: UMLS:C0020540 {source="MONDO:equivalentTo", source="MONDO:MEDGEN", source="MEDGEN:9374"}
 is_a: MONDO:0005044 {source="DOID:10824", source="EFO:1001031", source="MESH:D006974"} ! hypertensive disorder
-property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8004" xsd:string
+property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/8004" xsd:anyURI
 
 [Term]
 id: MONDO:0006847
@@ -309898,7 +309898,7 @@ subset: ordo_malformation_syndrome {source="Orphanet:280576"}
 subset: orphanet_rare {source="Orphanet:280576"}
 subset: otar {source="MONDO:OTAR"}
 subset: rare
-synonym: "BANF1-related neurodevelopmental syndrome" EXACT CLINGEN_LABEL [https://search.clinicalgenome.org/CCID\:008387]
+synonym: "BANF1-related neurodevelopmental syndrome" EXACT CLINGEN_LABEL [https://search.clinicalgenome.org/CCID:008387]
 synonym: "Nestor-Guillermo progeria syndrome" EXACT [MONDO:Lexical, OMIM:614008]
 synonym: "NGPS" EXACT ABBREVIATION [MONDO:Lexical, OMIM:614008, Orphanet:280576]
 synonym: "progeria syndrome, childhood-onset, with osteolysis" RELATED [OMIM:614008]