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DESCRIBE <http://purl.uniprot.org/SHA-384/04B0F985ED27EEFF83075717DB37B688BDF0481D143A0AE94065BF69806EDDD8174534DD08E2FD08238A92641D7165D3>
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http://purl.uniprot.org/SHA-384/04B0F985ED27EEFF83075717DB37B688BDF0481D143A0AE94065BF69806EDDD8174534DD08E2FD08238A92641D7165D3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/04B0F985ED27EEFF83075717DB37B688BDF0481D143A0AE94065BF69806EDDD8174534DD08E2FD08238A92641D7165D3
http://www.w3.org/2000/01/rdf-schema#comment
"loss-of-function mutations in MDH2 are also associated with severe neurological clinical presentations in children"
xsd:string
http://purl.uniprot.org/uniprot/#_0F8B9255B90055F313D8282DFFBB54F783DAFDCC70018DFC569BE548AB0980080B89D2D6C9E26C1A6B22A17E928A6C92
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/04B0F985ED27EEFF83075717DB37B688BDF0481D143A0AE94065BF69806EDDD8174534DD08E2FD08238A92641D7165D3
http://purl.uniprot.org/uniprot/Q75MT9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/04B0F985ED27EEFF83075717DB37B688BDF0481D143A0AE94065BF69806EDDD8174534DD08E2FD08238A92641D7165D3
http://purl.uniprot.org/uniprot/#_Q75MT9-mappedCitation-27989324
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/04B0F985ED27EEFF83075717DB37B688BDF0481D143A0AE94065BF69806EDDD8174534DD08E2FD08238A92641D7165D3