RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/SHA-384/CC797A1D18A646A814DE7181DC324ACC24BC18F3EEC8ED5299391037E9FE9D8E7D7B3924DAFED6BE573AD9F1DC76249Chttp://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CC797A1D18A646A814DE7181DC324ACC24BC18F3EEC8ED5299391037E9FE9D8E7D7B3924DAFED6BE573AD9F1DC76249Chttp://www.w3.org/2000/01/rdf-schema#comment"we found 2 additional patients carrying compound heterozygous variants in GFER. Reverse phenotyping confirmed the phenotypical similarities between the 4 patients. Together with the first literature reports the review of these 8 cases from 4 unrelated families enables us to better describe this apparently homogeneous disorder with the clinical and biological stigmata of mitochondrial disease"xsd:string
http://purl.uniprot.org/uniprot/#_291F3ACB8905E6234635411A97F3E69E953A16FB4EFA007377E365A0DD3012EC10FAF56B0216F9F8AB217960CF43DC3Fhttp://www.w3.org/1999/02/22-rdf-syntax-ns#subjecthttp://purl.uniprot.org/SHA-384/CC797A1D18A646A814DE7181DC324ACC24BC18F3EEC8ED5299391037E9FE9D8E7D7B3924DAFED6BE573AD9F1DC76249C
http://purl.uniprot.org/uniprot/Q9H2X5http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/CC797A1D18A646A814DE7181DC324ACC24BC18F3EEC8ED5299391037E9FE9D8E7D7B3924DAFED6BE573AD9F1DC76249C
http://purl.uniprot.org/uniprot/#_Q9H2X5-mappedCitation-28155230http://purl.uniprot.org/core/mappedAnnotationhttp://purl.uniprot.org/SHA-384/CC797A1D18A646A814DE7181DC324ACC24BC18F3EEC8ED5299391037E9FE9D8E7D7B3924DAFED6BE573AD9F1DC76249C