exclude superclasses from 'juvenile myoclonic epilepsy'

close #8465

src/ontology/mondo-edit.obo

@@ -210438,15 +210438,15 @@ xref: Orphanet:307 {source="MONDO:equivalentTo", source="OMIM:254770"}
 xref: Orphanet:862 {source="DOID:4890"}
 xref: SCTID:6204001 {source="MONDO:equivalentTo", source="DOID:4890"}
 xref: UMLS:C0270853 {source="MEDGEN:78738", source="MONDO:equivalentTo", source="MONDO:MEDGEN"}
-is_a: MONDO:0000415 {source="DOID:4890"} ! adolescence-adult electroclinical syndrome
 is_a: MONDO:0005027 {source="DOID:4890/inferred", source="MESH:D020190/inferred", source="MONDO:Redundant", source="NCIT:C84796"} ! epilepsy
 is_a: MONDO:0005579 {source="https://www.epilepsydiagnosis.org/epilepsy/generalized-epilepsy-groupoverview.html"} ! idiopathic generalized epilepsy
-is_a: MONDO:0017704 {source="Orphanet:307"} ! familial partial epilepsy
-is_a: MONDO:0100030 {source="https://orcid.org/0000-0001-8486-0558"} ! adolescent/adult-onset epilepsy syndrome
 relationship: disease_has_feature HP:0001336 ! Myoclonus
 relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/general/qc-single-child.sparql
 relationship: excluded_from_qc_check http://purl.obolibrary.org/obo/mondo/sparql/qc/mondo/qc-omim-subsumption.sparql
+relationship: excluded_subClassOf MONDO:0000415 {source="DOID:4890"} ! adolescence-adult electroclinical syndrome
 relationship: excluded_subClassOf MONDO:0005395 {source="MONDO:0017652-obsoleted", source="https://orcid.org/0000-0001-5208-3432"} ! movement disorder
+relationship: excluded_subClassOf MONDO:0017704 {source="Orphanet:307"} ! familial partial epilepsy
+relationship: excluded_subClassOf MONDO:0100030 {source="https://orcid.org/0000-0001-8486-0558"} ! adolescent/adult-onset epilepsy syndrome
 relationship: has_characteristic MONDO:0021152 {source="OMIMPS:254770"} ! inherited
 property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/6808/juvenile-myoclonic-epilepsy" xsd:anyURI {source="GARD:0006808"}
 property_value: seeAlso "https://www.epilepsydiagnosis.org/syndrome/jme-overview.html" xsd:anyURI