Fix DOID:0060822 definition (chromosomal location of gene)

Closes #1377

src/ontology/doid-edit.owl

@@ -39439,7 +39439,7 @@ SubClassOf(obo:DOID_0060821 obo:DOID_0060309)
 
 # Class: obo:DOID_0060822 (syndromic X-linked intellectual disability Cabezas type)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/10978355") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/17236139") obo:IAO_0000115 obo:DOID_0060822 "A syndromic X-linked intellectual disability characterized by intellectual deficit, muscle wasting, short stature, hypogonadism, and abnormal gait, with variable occurrence of prominent lower lip, kyphosis, joint hyperextensibility, tremor, decreased fine motor coordination and impaired speech that has_material_basis_in mutation in the CUL4B gene on chromosome Xq23."@en)
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/10978355") Annotation(oboInOwl:hasDbXref "url:https://www.ncbi.nlm.nih.gov/pubmed/17236139") obo:IAO_0000115 obo:DOID_0060822 "A syndromic X-linked intellectual disability characterized by intellectual deficit, muscle wasting, short stature, hypogonadism, and abnormal gait, with variable occurrence of prominent lower lip, kyphosis, joint hyperextensibility, tremor, decreased fine motor coordination and impaired speech that has_material_basis_in mutation in the CUL4B gene on chromosome Xq24."@en)
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060822 "GARD:13244")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060822 "ICD10CM:Q87.8")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0060822 "MIM:300354")