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DESCRIBE <http://purl.uniprot.org/SHA-384/89EE64F6D22F6BBA2860FBD12A35220C14733E6F711A4371736E43974C762320BF947A1908DF3B860C75CA015D6EB074>
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http://purl.uniprot.org/SHA-384/89EE64F6D22F6BBA2860FBD12A35220C14733E6F711A4371736E43974C762320BF947A1908DF3B860C75CA015D6EB074
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/89EE64F6D22F6BBA2860FBD12A35220C14733E6F711A4371736E43974C762320BF947A1908DF3B860C75CA015D6EB074
http://www.w3.org/2000/01/rdf-schema#comment
"The frequency of the pathogenic mutations in MFN2 gene detected in Czech hereditary motor and sensory neuropathy type II (HMSN II) patients was 7.2%."
xsd:string
http://purl.uniprot.org/uniprot/#_C0C81E2B09C5D451CE52FC052D9EFF6C818B11A49766DCBDC7B78F4FF3008CB998DF579FB86925E3D4603C1D2E41EDD0
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/89EE64F6D22F6BBA2860FBD12A35220C14733E6F711A4371736E43974C762320BF947A1908DF3B860C75CA015D6EB074
http://purl.uniprot.org/uniprot/O95140
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/89EE64F6D22F6BBA2860FBD12A35220C14733E6F711A4371736E43974C762320BF947A1908DF3B860C75CA015D6EB074
http://purl.uniprot.org/uniprot/#_O95140-mappedCitation-24126688
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/89EE64F6D22F6BBA2860FBD12A35220C14733E6F711A4371736E43974C762320BF947A1908DF3B860C75CA015D6EB074