<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"Neutral 1 amino acid transport defect"@en .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:234500"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"deficiency of tryptophan oxygenase"@en .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#inSubset>	<http://purl.obolibrary.org/obo/doid#NCIthesaurus> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:80902009"^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50947055	<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_1060>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	_:vb50947055 .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ICD10CM:E72.02"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.w3.org/1999/02/22-rdf-syntax-ns#type>	<http://www.w3.org/2002/07/owl#Class> .
_:vb50947055	<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_1060>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C0018609"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.w3.org/2000/01/rdf-schema#comment>	"OMIM mapping confirmed by DO. [SN]."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"neutral amino acid transport defect"@en .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:6569"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<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_1060>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:1060"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_9252> .
_:vb50947055	<http://www.w3.org/2002/07/owl#someValuesFrom>	<http://purl.obolibrary.org/obo/HP_0003355> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://purl.obolibrary.org/obo/IAO_0000115>	"An amino acid metabolic disorder that is caused by abnormalities of the renal tubules and is characterized especially by aminoaciduria involving only monocarboxylic monoamines, a dry red scaly rash, and episodic muscular incoordination due to the effects of the disease on the cerebellum."^^<http://www.w3.org/2001/XMLSchema#string> .
_:vb50947055	<http://www.w3.org/2002/07/owl#onProperty>	<http://purl.obolibrary.org/obo/RO_0002200> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"NCI:C84748"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:D006250"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_1060>	<http://www.w3.org/2000/01/rdf-schema#label>	"Hartnup disease"^^<http://www.w3.org/2001/XMLSchema#string> .