<http://purl.obolibrary.org/obo/DOID_0111329>	<http://purl.obolibrary.org/obo/IAO_0000115>	"A vitamin metabolic disorder characterized by vitamin B6 deficienc resulting in neonatal-onset of severe seizures that can be controlled with pyridoxal 5'-phosphate treatment that has_material_basis_in homozygous or compound heterozygous mutation in PNPO on 17q21.32."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"pyridoxal phosphate-dependent seizures"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"SNOMEDCT_US_2021_09_01:724576005"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"pyridoxal phosphate-responsive seizures"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"PNPO-related neonatal epileptic encephalopathy"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"ORDO:79096"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<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_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"UMLS_CUI:C1864723"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<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_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"PNPO deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.w3.org/2000/01/rdf-schema#subClassOf>	<http://purl.obolibrary.org/obo/DOID_0050718> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"OMIM:610090"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#id>	"DOID:0111329"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"pyridoxamine 5-prime-phosphate oxidase deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"GARD:10730"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.w3.org/2000/01/rdf-schema#label>	"pyridoxamine 5'-phosphate oxidase deficiency"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"pyridoxamine 5'-oxidase deficiency"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasExactSynonym>	"pyridoxal 5'-phosphate-dependent epilepsy"@en .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasOBONamespace>	"disease_ontology"^^<http://www.w3.org/2001/XMLSchema#string> .
<http://purl.obolibrary.org/obo/DOID_0111329>	<http://www.geneontology.org/formats/oboInOwl#hasDbXref>	"MESH:C566449"^^<http://www.w3.org/2001/XMLSchema#string> .