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DESCRIBE <http://purl.uniprot.org/SHA-384/4C1C82858A204E8CEFC92398143378ADB0737617993C7539F64A5C87B70EFA2886A20E55DE6D79C35B1452CA48D0D19D>
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http://purl.uniprot.org/SHA-384/4C1C82858A204E8CEFC92398143378ADB0737617993C7539F64A5C87B70EFA2886A20E55DE6D79C35B1452CA48D0D19D
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4C1C82858A204E8CEFC92398143378ADB0737617993C7539F64A5C87B70EFA2886A20E55DE6D79C35B1452CA48D0D19D
http://www.w3.org/2000/01/rdf-schema#comment
"Rett Syndrome a Neurodevelopmental Disorder Whole-Transcriptome and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways."
xsd:string
http://purl.uniprot.org/uniprot/#_351E0F2CF2F792DA01DAF7FB66F5C7707647DFE3EF2E28702F520BCA9E3E8EDC48A7D6D48605F2DE4CDBD1A967816C20
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4C1C82858A204E8CEFC92398143378ADB0737617993C7539F64A5C87B70EFA2886A20E55DE6D79C35B1452CA48D0D19D
http://purl.uniprot.org/uniprot/P55316
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4C1C82858A204E8CEFC92398143378ADB0737617993C7539F64A5C87B70EFA2886A20E55DE6D79C35B1452CA48D0D19D
http://purl.uniprot.org/uniprot/#_P55316-mappedCitation-32105570
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4C1C82858A204E8CEFC92398143378ADB0737617993C7539F64A5C87B70EFA2886A20E55DE6D79C35B1452CA48D0D19D