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DESCRIBE <http://purl.uniprot.org/SHA-384/B908DF8D5F5717D047BDE827436B6A6735A1D89E67A339E3AF8BEE2D9AE6897F70C1C3516AA01B3F76EFA64500F36F02>
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http://purl.uniprot.org/SHA-384/B908DF8D5F5717D047BDE827436B6A6735A1D89E67A339E3AF8BEE2D9AE6897F70C1C3516AA01B3F76EFA64500F36F02
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B908DF8D5F5717D047BDE827436B6A6735A1D89E67A339E3AF8BEE2D9AE6897F70C1C3516AA01B3F76EFA64500F36F02
http://www.w3.org/2000/01/rdf-schema#comment
"Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish."
xsd:string
http://purl.uniprot.org/uniprot/#_C9F74D54D8F2C869151E20EABDB33166542ACB5981AAB4F151F0EDF569F06F6BA351C117ACE11022E47B5EDB99E3629A
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B908DF8D5F5717D047BDE827436B6A6735A1D89E67A339E3AF8BEE2D9AE6897F70C1C3516AA01B3F76EFA64500F36F02
http://purl.uniprot.org/uniprot/Q9HA31
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B908DF8D5F5717D047BDE827436B6A6735A1D89E67A339E3AF8BEE2D9AE6897F70C1C3516AA01B3F76EFA64500F36F02
http://purl.uniprot.org/uniprot/#_Q9HA31-mappedCitation-33517449
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B908DF8D5F5717D047BDE827436B6A6735A1D89E67A339E3AF8BEE2D9AE6897F70C1C3516AA01B3F76EFA64500F36F02