Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Dicarboxylic_aminoaciduria> ?p ?o }
- Dicarboxylic_aminoaciduria omim "222730".
- Dicarboxylic_aminoaciduria orpha "ORPHA2195".
- Dicarboxylic_aminoaciduria path "PBB/6505".
- Dicarboxylic_aminoaciduria symbol "SLC1A1".
- Dicarboxylic_aminoaciduria wikiPageUsesTemplate Template:GNF_Protein_box.
- Dicarboxylic_aminoaciduria wikiPageUsesTemplate Template:Infobox_disease.
- Dicarboxylic_aminoaciduria wikiPageUsesTemplate Template:Reflist.
- Dicarboxylic_aminoaciduria wikiPageUsesTemplate Template:Unicode.
- Dicarboxylic_aminoaciduria subject Category:Amino_acid_metabolism_disorders.
- Dicarboxylic_aminoaciduria subject Category:Autosomal_recessive_disorders.
- Dicarboxylic_aminoaciduria hypernym Form.
- Dicarboxylic_aminoaciduria type Disease.
- Dicarboxylic_aminoaciduria type Thing.
- Dicarboxylic_aminoaciduria type Q12136.
- Dicarboxylic_aminoaciduria comment "Dicarboxylic aminoaciduria is a rare form of aminoaciduria (1:35 000 births) which is an autosomal recessive disorder of urinary glutamate and aspartate due to genetic errors related to transport of these amino acids. Mutations resulting in a lack of expression of the SLC1A1 gene, a member of the solute carrier family, are found to cause development of dicarboxylic aminoaciduria in humans. SLC1A1 encodes for EAAT3 which is found in the neurons, intestine, kidney, lung, and heart.".
- Dicarboxylic_aminoaciduria label "Dicarboxylic aminoaciduria".
- Dicarboxylic_aminoaciduria sameAs m.02kb_ql.
- Dicarboxylic_aminoaciduria sameAs Q16252204.
- Dicarboxylic_aminoaciduria sameAs Q16252204.
- Dicarboxylic_aminoaciduria wasDerivedFrom Dicarboxylic_aminoaciduria?oldid=595148867.
- Dicarboxylic_aminoaciduria depiction PBB_GE_SLC1A1_213664_at_tn.png.
- Dicarboxylic_aminoaciduria isPrimaryTopicOf Dicarboxylic_aminoaciduria.
- Dicarboxylic_aminoaciduria name "Dicarboxylic aminoaciduria".