Reclassify and update DOID:0070652

Based on a recently accepted publication.

See #1523

Author: allenbaron

src/ontology/doid-edit.owl

@@ -53577,14 +53577,15 @@ SubClassOf(obo:DOID_0070651 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0070652 (Nil-Deshwan neurodevelopmental syndrome)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pmc.ncbi.nlm.nih.gov/articles/PMC10645550/") obo:IAO_0000115 obo:DOID_0070652 "A syndromic intellectual disability characterized by a range of congenital anomalies and central nervous system dysfunction, including global developmental delay, feeding difficulties, hypotonia, and impaired intellectual development that has_material_basis_in heterozygous mutation in the DOT1L gene on chromosome 19p13.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pmc.ncbi.nlm.nih.gov/articles/PMC10645550/") Annotation(oboInOwl:hasDbXref "url: https://pubmed.ncbi.nlm.nih.gov/40494548/") obo:IAO_0000115 obo:DOID_0070652 "A syndrome characterized by a range of congenital anomalies and central nervous system dysfunction, including global developmental delay, feeding difficulties, hypotonia, and impaired intellectual development that has_material_basis_in heterozygous mutation in the DOT1L gene on chromosome 19p13.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0070652 "MIM:621265")
 AnnotationAssertion(oboInOwl:hasOBONamespace obo:DOID_0070652 "disease_ontology")
 AnnotationAssertion(oboInOwl:id obo:DOID_0070652 "DOID:0070652")
 AnnotationAssertion(oboInOwl:inSubset obo:DOID_0070652 doid:DO_rare_slim)
 AnnotationAssertion(rdfs:label obo:DOID_0070652 "Nil-Deshwan neurodevelopmental syndrome")
 AnnotationAssertion(skos:exactMatch obo:DOID_0070652 "MIM:621265")
-SubClassOf(obo:DOID_0070652 obo:DOID_0050888)
+SubClassOf(obo:DOID_0070652 obo:DOID_225)
+SubClassOf(obo:DOID_0070652 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_0000147))
 
 # Class: obo:DOID_0070653 (Fliedner-Zweier syndrome)