Fix lissencephaly 1 definition

Author: allenbaron

src/ontology/doid-edit.owl

@@ -102182,7 +102182,7 @@ SubClassOf(obo:DOID_0112236 ObjectSomeValuesFrom(obo:IDO_0000664 obo:GENO_000014
 
 # Class: obo:DOID_0112237 (lissencephaly 1)
 
-AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/11754098/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/12668601/") obo:IAO_0000115 obo:DOID_0112237 "A lissencephaly characterized by an abnormally thick cortex, reduced or abnormal lamination, and diffuse neuronal heterotopia that has_material_basis_in mutation heterozygous in the PAFAH1B1 gene on chromosome 17p13.3.")
+AnnotationAssertion(Annotation(dc:type obo:ECO_0007645) Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/11754098/") Annotation(oboInOwl:hasDbXref "url:https://pubmed.ncbi.nlm.nih.gov/12668601/") obo:IAO_0000115 obo:DOID_0112237 "A lissencephaly characterized by an abnormally thick cortex, reduced or abnormal lamination, and diffuse neuronal heterotopia that has_material_basis_in heterozygous mutation in the PAFAH1B1 gene on chromosome 17p13.3.")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0112237 "MIM:607432")
 AnnotationAssertion(oboInOwl:hasDbXref obo:DOID_0112237 "ORDO:95232")
 AnnotationAssertion(Annotation(oboInOwl:hasSynonymType obo:OMO_0003012) oboInOwl:hasExactSynonym obo:DOID_0112237 "LIS1")