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DESCRIBE <http://purl.uniprot.org/SHA-384/1F52A9CD808C2FDFE488F384C23BE1414B2063F200A5655DA2ECCC442EE19D721565B019B5A3A84655A16A483A120E08>
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http://purl.uniprot.org/SHA-384/1F52A9CD808C2FDFE488F384C23BE1414B2063F200A5655DA2ECCC442EE19D721565B019B5A3A84655A16A483A120E08
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/1F52A9CD808C2FDFE488F384C23BE1414B2063F200A5655DA2ECCC442EE19D721565B019B5A3A84655A16A483A120E08
http://www.w3.org/2000/01/rdf-schema#comment
"In this family with a mutation in IMPDH1 we found a specific phenotype with rod function affected more than cone function foveal edema and central retinal function preserved for a long period of time."
xsd:string
http://purl.uniprot.org/uniprot/#_2340E06FA420959AADAE5E76AA2013C83C50E8ABDCB852FDA0801C2401AC7D893B43347B0B11BCE17157ADD6AD6DE138
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/1F52A9CD808C2FDFE488F384C23BE1414B2063F200A5655DA2ECCC442EE19D721565B019B5A3A84655A16A483A120E08
http://purl.uniprot.org/uniprot/Q5H9Q6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1F52A9CD808C2FDFE488F384C23BE1414B2063F200A5655DA2ECCC442EE19D721565B019B5A3A84655A16A483A120E08
http://purl.uniprot.org/uniprot/#_Q5H9Q6-mappedCitation-16272056
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/1F52A9CD808C2FDFE488F384C23BE1414B2063F200A5655DA2ECCC442EE19D721565B019B5A3A84655A16A483A120E08