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DESCRIBE <http://purl.uniprot.org/SHA-384/68C100912199873BE679A53F2B585E527C72416BAB5173F8FA8D2CB0A7ADAF38957C034A03C15D6E3DB4B83491B43762>
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http://purl.uniprot.org/SHA-384/68C100912199873BE679A53F2B585E527C72416BAB5173F8FA8D2CB0A7ADAF38957C034A03C15D6E3DB4B83491B43762
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/68C100912199873BE679A53F2B585E527C72416BAB5173F8FA8D2CB0A7ADAF38957C034A03C15D6E3DB4B83491B43762
http://www.w3.org/2000/01/rdf-schema#comment
"Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder."
xsd:string
http://purl.uniprot.org/uniprot/#_936E52616C5BF5DDFFD707C1675138B6FA6DC9A4BF3126A5DF64AEC547734A6C42A39C921FA4DB2FFC7CDB9E7DD80608
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/68C100912199873BE679A53F2B585E527C72416BAB5173F8FA8D2CB0A7ADAF38957C034A03C15D6E3DB4B83491B43762
http://purl.uniprot.org/uniprot/Q58EZ8
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/68C100912199873BE679A53F2B585E527C72416BAB5173F8FA8D2CB0A7ADAF38957C034A03C15D6E3DB4B83491B43762
http://purl.uniprot.org/uniprot/#_Q58EZ8-mappedCitation-33963192
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/68C100912199873BE679A53F2B585E527C72416BAB5173F8FA8D2CB0A7ADAF38957C034A03C15D6E3DB4B83491B43762