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DESCRIBE <http://purl.uniprot.org/SHA-384/17B930EB458E0AEBF5352BBBDEDD5C41AFBE5B1F7E121AEECA1604C32A9FCA97473A2341FA36775BBB96FFCE4ED75CD2>
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http://purl.uniprot.org/SHA-384/17B930EB458E0AEBF5352BBBDEDD5C41AFBE5B1F7E121AEECA1604C32A9FCA97473A2341FA36775BBB96FFCE4ED75CD2
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/17B930EB458E0AEBF5352BBBDEDD5C41AFBE5B1F7E121AEECA1604C32A9FCA97473A2341FA36775BBB96FFCE4ED75CD2
http://www.w3.org/2000/01/rdf-schema#comment
"MTO1 mutations are commonly associated with a presentation of hypertrophic cardiomyopathy lactic acidosis and MRC deficiency."
xsd:string
http://purl.uniprot.org/uniprot/#_983383573998B7507005586C2BBE10B6CB25374FA23594EC7094425F87E0A8D456D6561CF0681837FE778E1CDAF0BA7A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/17B930EB458E0AEBF5352BBBDEDD5C41AFBE5B1F7E121AEECA1604C32A9FCA97473A2341FA36775BBB96FFCE4ED75CD2
http://purl.uniprot.org/uniprot/Q9Y2Z2
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/17B930EB458E0AEBF5352BBBDEDD5C41AFBE5B1F7E121AEECA1604C32A9FCA97473A2341FA36775BBB96FFCE4ED75CD2
http://purl.uniprot.org/uniprot/#_Q9Y2Z2-mappedCitation-23929671
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/17B930EB458E0AEBF5352BBBDEDD5C41AFBE5B1F7E121AEECA1604C32A9FCA97473A2341FA36775BBB96FFCE4ED75CD2