<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E78.3"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938708	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0004019> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:246700"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#created_by>	"elvira"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938708	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Restriction> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0795956"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Anderson disease"@en .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50938708 .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:702364003"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C535460"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_3146> .
_:vb50938708	<http://www.w3.org/2007/05/powder-s#describedby>	<https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:71"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#creation_date>	"2015-08-20T12:44:44Z"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0060357"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#DO_rare_slim> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:9683"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50938708	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/SO_0001537> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"CMRD"@en .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A lipid metabolism disorder characterized by malnutrition, failure to thrive, growth failure, vitamin E deficiency and the absence of chylomicrons and apolipoprotein B48 post-prandially. It has an autosomal recessive inheritance pattern and has_material_basis_in mutations in the SAR1B gene on chromosome 5q31.1."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0060357>	<http://www.w3.org/2000/01/rdf-schema#label>	"chylomicron retention disease"^^<http://www.w3.org/2001/XMLSchema#string> .