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DESCRIBE <http://purl.uniprot.org/SHA-384/CE52FF2D37D33246C08870507D7F36B2FA4347F71F860E9295465298C31709BB8F07CA450F495C0A5555F737A3A0578C>
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http://purl.uniprot.org/SHA-384/CE52FF2D37D33246C08870507D7F36B2FA4347F71F860E9295465298C31709BB8F07CA450F495C0A5555F737A3A0578C
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CE52FF2D37D33246C08870507D7F36B2FA4347F71F860E9295465298C31709BB8F07CA450F495C0A5555F737A3A0578C
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); WNT8b and SHH mutations and abnormal expressions are present in the peripheral blood of children with sporadic Hirschsprung disease."
xsd:string
http://purl.uniprot.org/uniprot/#_BEDD3F0F1AF92B9E5B4227E3E09C2C6E3F6CEEAFA1E641AC4193CDAF5F305B274C55F2DB00C1F3D58952C6482480756E
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CE52FF2D37D33246C08870507D7F36B2FA4347F71F860E9295465298C31709BB8F07CA450F495C0A5555F737A3A0578C
http://purl.uniprot.org/uniprot/Q93098
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CE52FF2D37D33246C08870507D7F36B2FA4347F71F860E9295465298C31709BB8F07CA450F495C0A5555F737A3A0578C
http://purl.uniprot.org/uniprot/#_Q93098-mappedCitation-20972907
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CE52FF2D37D33246C08870507D7F36B2FA4347F71F860E9295465298C31709BB8F07CA450F495C0A5555F737A3A0578C