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DESCRIBE <http://purl.uniprot.org/SHA-384/46409609CB70F6190759913393754EEAF0A13DC705ED4A8D517A5F093C322558A66523C5C1B47E348E17BA496C2CA216>
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http://purl.uniprot.org/SHA-384/46409609CB70F6190759913393754EEAF0A13DC705ED4A8D517A5F093C322558A66523C5C1B47E348E17BA496C2CA216
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/46409609CB70F6190759913393754EEAF0A13DC705ED4A8D517A5F093C322558A66523C5C1B47E348E17BA496C2CA216
http://www.w3.org/2000/01/rdf-schema#comment
"Data indicate that most of patients with Congenital bilateral absence of the vas deferens (CBAVD) have mutations in the CFTR gene; Observational study of genotype prevalence. (HuGE Navigator)"
xsd:string
http://purl.uniprot.org/uniprot/#_F29DCFD749D6CECC20B670D4B00DC0D934AD1E550559C679D36E24A2964C39AD4AE0F83893635F4C21B9EACF83BCB0A2
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/46409609CB70F6190759913393754EEAF0A13DC705ED4A8D517A5F093C322558A66523C5C1B47E348E17BA496C2CA216
http://purl.uniprot.org/uniprot/Q6KEG9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/46409609CB70F6190759913393754EEAF0A13DC705ED4A8D517A5F093C322558A66523C5C1B47E348E17BA496C2CA216
http://purl.uniprot.org/uniprot/#_Q6KEG9-mappedCitation-16714368
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/46409609CB70F6190759913393754EEAF0A13DC705ED4A8D517A5F093C322558A66523C5C1B47E348E17BA496C2CA216