_:vb50938516	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50938516	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0060233> .
_:vb50938516	<http://www.w3.org/2002/07/owl#annotatedTarget>	"A RASopathy characterized by unusually sparse, brittle, curly hair, macrocephaly, a prominent forehead and bi-temporal narrowing, intellectual disability, failure to thrive, congenital heart defects, short stature and skin abnormalities, and has_material_basis_in mutation in the BRAF, MAP2K1, MAP2kK2 and KRAS genes."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938516	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://ghr.nlm.nih.gov/condition/cardiofaciocutaneous-syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938516	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50938516	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007636> .
_:vb50938516	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007637> .
_:vb50938516	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007638> .
_:vb50938516	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:https://www.rarediseases.org/rare-disease-information/rare-diseases/byID/877/viewAbstract"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938516	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50938516	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://en.wikipedia.org/wiki/Cardiofaciocutaneous_syndrome"^^<http://www.w3.org/2001/XMLSchema#string> .