_:vb50938828	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938828	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50938828	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A syndrome that has_material_basis_in genetic changes that affect the SATB2 gene and that is characterized by mild to severe intellectual disability, a delayed or absent ability to speak,  severe speech anomalies, abnormalities of the palate, teeth anomalies, behavioral issues with or without bone or brain anomalies, and onset before age 2."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938828	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.ncbi.nlm.nih.gov/books/NBK458647/"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938828	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://ghr.nlm.nih.gov/condition/satb2-associated-syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938828	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50938828	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0060428> .