| http://purl.uniprot.org/uniprot/Q92947 | http://purl.uniprot.org/core/classifiedWith | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/2000/01/rdf-schema#subClassOf | http://purl.uniprot.org/keywords/9995 |
| http://purl.uniprot.org/keywords/316 | http://purl.uniprot.org/core/category | http://purl.uniprot.org/keywords/9995 |
| http://purl.uniprot.org/diseases/515 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/diseases/514 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/keywords/9995 | http://www.w3.org/2004/02/skos/core#narrower | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/2004/02/skos/core#prefLabel | "Glutaricaciduria"xsd:string |
| http://purl.uniprot.org/diseases/513 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/uniprot/P13804 | http://purl.uniprot.org/core/classifiedWith | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/uniprot/P38117 | http://purl.uniprot.org/core/classifiedWith | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/2004/02/skos/core#altLabel | "GA"xsd:string |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Concept |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/2000/01/rdf-schema#subClassOf | http://purl.uniprot.org/core/Concept |
| http://purl.uniprot.org/diseases/516 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/uniprot/Q16134 | http://purl.uniprot.org/core/classifiedWith | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/uniprot/Q9HAC7 | http://purl.uniprot.org/core/classifiedWith | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/diseases/512 | http://www.w3.org/2000/01/rdf-schema#seeAlso | http://purl.uniprot.org/keywords/316 |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/2000/01/rdf-schema#comment | "Protein which, if defective, causes glutaricaciduria (GA), a metabolic disorder characterized by the excretion of glutaric acid in the urine. Type I GA is caused by the deficiency of glutaryl-CoA dehydrogenase, a mitochondrial enzyme involved in the metabolism of lysine, hydroxylysine and tryptophan. Type II GA differs from type I in that multiple acyl-CoA dehydrogenase deficiencies result in a large excretion not only of glutaric acid but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. GA II can result from a deficiency of any one of 3 mitochondrial molecules: the alpha and beta subunits of electron transfer flavoprotein and electron transfer flavoprotein-ubiquinone oxidoreductase."xsd:string |
| http://purl.uniprot.org/keywords/316 | http://www.w3.org/2004/02/skos/core#altLabel | "Glutaric aciduria"xsd:string |