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DESCRIBE <http://purl.uniprot.org/SHA-384/2FB404F8620E188EE5909FCD558EAE6A6684685BD89F8D2D9EBC91026DD5507FB5455FF7AE59361AE8E9D39917A8C2E6>
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http://purl.uniprot.org/SHA-384/2FB404F8620E188EE5909FCD558EAE6A6684685BD89F8D2D9EBC91026DD5507FB5455FF7AE59361AE8E9D39917A8C2E6
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/2FB404F8620E188EE5909FCD558EAE6A6684685BD89F8D2D9EBC91026DD5507FB5455FF7AE59361AE8E9D39917A8C2E6
http://www.w3.org/2000/01/rdf-schema#comment
"GHRH mutations were not identified in a selected cohort of patients with isolated GH deficiency suggesting that if they exist they may be an extremely rare cause of isolated GH deficiency."
xsd:string
http://purl.uniprot.org/uniprot/#_7E65B9C64EA5934AE2FC12A27C9484BDD6E0803D0008536EE2FDE420C4C3018E6849EECD2DD4CCADEAAD320193044FA3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/2FB404F8620E188EE5909FCD558EAE6A6684685BD89F8D2D9EBC91026DD5507FB5455FF7AE59361AE8E9D39917A8C2E6
http://purl.uniprot.org/uniprot/P01286
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2FB404F8620E188EE5909FCD558EAE6A6684685BD89F8D2D9EBC91026DD5507FB5455FF7AE59361AE8E9D39917A8C2E6
http://purl.uniprot.org/uniprot/#_P01286-mappedCitation-21715545
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/2FB404F8620E188EE5909FCD558EAE6A6684685BD89F8D2D9EBC91026DD5507FB5455FF7AE59361AE8E9D39917A8C2E6