_:vb50937446	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
_:vb50937446	<http://www.w3.org/2002/07/owl#annotatedSource>	<http://purl.obolibrary.org/obo/DOID_0050710> .
_:vb50937446	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007638> .
_:vb50937446	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://en.wikipedia.org/wiki/3-Methylcrotonyl-CoA_carboxylase_deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50937446	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Axiom> .
_:vb50937446	<http://www.w3.org/2002/07/owl#annotatedProperty>	<http://purl.obolibrary.org/obo/IAO_0000115> .
_:vb50937446	<http://purl.org/dc/elements/1.1/type>	<http://purl.obolibrary.org/obo/ECO_0007636> .
_:vb50937446	<http://www.w3.org/2002/07/owl#annotatedTarget>	"An amino acid metabolic disorder that is classified by inadequate levels of the enzyme 3-methylcrotonyl-CoA carboxylase that helps break down proteins containing the amino acid leucine. This disease has_symptom muscular hypotonia (weak muscle tone), has_symptom muscular atrophy, has_symptom feeding difficulties, has_symptom recurrent episodes of vomiting and diarrhea, and has_symptom lethargy."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50937446	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"url:http://omim.org/entry/210200"^^<http://www.w3.org/2001/XMLSchema#string> .