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DESCRIBE <http://purl.uniprot.org/SHA-384/20EFB802AB341DEF0FCEED97E2DC4D3DE4891986C2FBDE0B371A3BEF09A8EF3D5A4BBBDFE13E1ED3B94EEA7CB65838D7>
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http://purl.uniprot.org/SHA-384/20EFB802AB341DEF0FCEED97E2DC4D3DE4891986C2FBDE0B371A3BEF09A8EF3D5A4BBBDFE13E1ED3B94EEA7CB65838D7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/20EFB802AB341DEF0FCEED97E2DC4D3DE4891986C2FBDE0B371A3BEF09A8EF3D5A4BBBDFE13E1ED3B94EEA7CB65838D7
http://www.w3.org/2000/01/rdf-schema#comment
"the neurodevelopmental phenotype of UPF3B missense mutation is caused by impairment of nonsense-mediated mRNA decay pathway function altering neuronal differentiation."
xsd:string
http://purl.uniprot.org/uniprot/#_C794A60FA67500B93985CCA5CD31BB31803768F668F0B9963288D2C676A7B31DE7123AFDCF05F9E74493977B0A88E5C1
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/20EFB802AB341DEF0FCEED97E2DC4D3DE4891986C2FBDE0B371A3BEF09A8EF3D5A4BBBDFE13E1ED3B94EEA7CB65838D7
http://purl.uniprot.org/uniprot/I3XIE4
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/20EFB802AB341DEF0FCEED97E2DC4D3DE4891986C2FBDE0B371A3BEF09A8EF3D5A4BBBDFE13E1ED3B94EEA7CB65838D7
http://purl.uniprot.org/uniprot/#_I3XIE4-mappedCitation-26012578
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/20EFB802AB341DEF0FCEED97E2DC4D3DE4891986C2FBDE0B371A3BEF09A8EF3D5A4BBBDFE13E1ED3B94EEA7CB65838D7