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DESCRIBE <http://purl.uniprot.org/SHA-384/B42BC4054216DBAF2F385B89DB4B46F1FA2CC2FF6030ABCED8255D4022DF335DF788BBA94CBFC44D154E39C2627F094D>
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http://purl.uniprot.org/SHA-384/B42BC4054216DBAF2F385B89DB4B46F1FA2CC2FF6030ABCED8255D4022DF335DF788BBA94CBFC44D154E39C2627F094D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B42BC4054216DBAF2F385B89DB4B46F1FA2CC2FF6030ABCED8255D4022DF335DF788BBA94CBFC44D154E39C2627F094D
http://www.w3.org/2000/01/rdf-schema#comment
"METT11D1 mutations could not explain phenotype of patients with combined oxidative phosphorylation system deficiencies."
xsd:string
http://purl.uniprot.org/uniprot/#_65EC1F2812BA40A3E74B15461E9F9C7C79F4F6FA4AFB09BFE0158279A79BCCC9A8452A3691D0B021DBDCC63C780A209B
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B42BC4054216DBAF2F385B89DB4B46F1FA2CC2FF6030ABCED8255D4022DF335DF788BBA94CBFC44D154E39C2627F094D
http://purl.uniprot.org/uniprot/A0A0S2Z5V5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B42BC4054216DBAF2F385B89DB4B46F1FA2CC2FF6030ABCED8255D4022DF335DF788BBA94CBFC44D154E39C2627F094D
http://purl.uniprot.org/uniprot/#_A0A0S2Z5V5-mappedCitation-24137763
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B42BC4054216DBAF2F385B89DB4B46F1FA2CC2FF6030ABCED8255D4022DF335DF788BBA94CBFC44D154E39C2627F094D