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DESCRIBE <http://purl.uniprot.org/SHA-384/B79C2D49DFD6705F85AA2D493C181916DAE2D3D7FE2FDEEA9D366A15C136A9438B8C08E43385C9041276F4C3AD7A1DBF>
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http://purl.uniprot.org/SHA-384/B79C2D49DFD6705F85AA2D493C181916DAE2D3D7FE2FDEEA9D366A15C136A9438B8C08E43385C9041276F4C3AD7A1DBF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B79C2D49DFD6705F85AA2D493C181916DAE2D3D7FE2FDEEA9D366A15C136A9438B8C08E43385C9041276F4C3AD7A1DBF
http://www.w3.org/2000/01/rdf-schema#comment
"Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders."
xsd:string
http://purl.uniprot.org/uniprot/#_A778FA0984E109151356C28DB8A9902593A4765E076FC4C081B244A69BC13956A703DBCBD791990DA3F0E1B2358BFA2D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B79C2D49DFD6705F85AA2D493C181916DAE2D3D7FE2FDEEA9D366A15C136A9438B8C08E43385C9041276F4C3AD7A1DBF
http://purl.uniprot.org/uniprot/Q6JH02
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B79C2D49DFD6705F85AA2D493C181916DAE2D3D7FE2FDEEA9D366A15C136A9438B8C08E43385C9041276F4C3AD7A1DBF
http://purl.uniprot.org/uniprot/#_Q6JH02-mappedCitation-35543142
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B79C2D49DFD6705F85AA2D493C181916DAE2D3D7FE2FDEEA9D366A15C136A9438B8C08E43385C9041276F4C3AD7A1DBF