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DESCRIBE <http://purl.uniprot.org/SHA-384/C3DA9201F5F76AB740DD143A79A5801F3176DC6747F74C886392DC7C036FC133D0D5C6FA90C810D348256FEF98E8F44F>
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http://purl.uniprot.org/SHA-384/C3DA9201F5F76AB740DD143A79A5801F3176DC6747F74C886392DC7C036FC133D0D5C6FA90C810D348256FEF98E8F44F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C3DA9201F5F76AB740DD143A79A5801F3176DC6747F74C886392DC7C036FC133D0D5C6FA90C810D348256FEF98E8F44F
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in the PROP1 and HESX1 genes were not identified in these patients with sporadic growth hormone defiency combined pituitary hormone deficiency and septo-optic dysplasia."
xsd:string
http://purl.uniprot.org/uniprot/#_1A3261214D97BDB529F6C9732DF4BC1C94CE963DDE9DAACB0446A44B17F0458E4D8553DC927D55620D556C71FA04D449
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C3DA9201F5F76AB740DD143A79A5801F3176DC6747F74C886392DC7C036FC133D0D5C6FA90C810D348256FEF98E8F44F
http://purl.uniprot.org/uniprot/Q9UBX0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C3DA9201F5F76AB740DD143A79A5801F3176DC6747F74C886392DC7C036FC133D0D5C6FA90C810D348256FEF98E8F44F
http://purl.uniprot.org/uniprot/#_Q9UBX0-mappedCitation-20694410
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C3DA9201F5F76AB740DD143A79A5801F3176DC6747F74C886392DC7C036FC133D0D5C6FA90C810D348256FEF98E8F44F