_:vb50948138	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50948138	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://www.ninds.nih.gov/disorders/rett/detail_rett.htm"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948138	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_1206> .
_:vb50948138	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://www.nichd.nih.gov/health/topics/rett_syndrome.cfm"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948138	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://medlineplus.gov/ency/article/001536.htm"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948138	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50948138	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007637> .
_:vb50948138	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50948138	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .