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DESCRIBE <http://purl.uniprot.org/SHA-384/E6E5055781192EDCF1E8B69758B1DBB56D6D9F95082C064720139529072CC4D767A87251570E0A49EFA268ABE163E262>
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http://purl.uniprot.org/SHA-384/E6E5055781192EDCF1E8B69758B1DBB56D6D9F95082C064720139529072CC4D767A87251570E0A49EFA268ABE163E262
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E6E5055781192EDCF1E8B69758B1DBB56D6D9F95082C064720139529072CC4D767A87251570E0A49EFA268ABE163E262
http://www.w3.org/2000/01/rdf-schema#comment
"In thyroid hemiagenesis genomic examinations revealed the presence of four recurrent defects (three deletions and one duplication) affecting highly conservative proteasome genes PSMA1 PSMA3 and PSMD3."
xsd:string
http://purl.uniprot.org/uniprot/#_A6DF01B12784AA62E407BAB7FF220CF3C32D192B9CA39BB263EA9A1D9F0193838DD23FB5E876CA786D71AB110E1B2A3D
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E6E5055781192EDCF1E8B69758B1DBB56D6D9F95082C064720139529072CC4D767A87251570E0A49EFA268ABE163E262
http://purl.uniprot.org/uniprot/A0A140VK43
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E6E5055781192EDCF1E8B69758B1DBB56D6D9F95082C064720139529072CC4D767A87251570E0A49EFA268ABE163E262
http://purl.uniprot.org/uniprot/#_A0A140VK43-mappedCitation-28390009
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E6E5055781192EDCF1E8B69758B1DBB56D6D9F95082C064720139529072CC4D767A87251570E0A49EFA268ABE163E262