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DESCRIBE <http://purl.uniprot.org/SHA-384/CA1D5715574BC6639F42E0D5D8985307A566D0873EC041C74DA9F51543ED92027EFF7998A3C5D178A8EF9EB52355414E>
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http://purl.uniprot.org/SHA-384/CA1D5715574BC6639F42E0D5D8985307A566D0873EC041C74DA9F51543ED92027EFF7998A3C5D178A8EF9EB52355414E
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CA1D5715574BC6639F42E0D5D8985307A566D0873EC041C74DA9F51543ED92027EFF7998A3C5D178A8EF9EB52355414E
http://www.w3.org/2000/01/rdf-schema#comment
"These results suggest that HNRNPU FAM36A and NCRNA00201 are not major genes for microcephaly and corpus callosum abnormalities but are good candidates for intellectual disability (ID) and seizures."
xsd:string
http://purl.uniprot.org/uniprot/#_679209835CC543EDB4702F26C085F11DA5A5233C447198B7D91854C1E3D486B95665D7C79F131085BB137725D9EE300F
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CA1D5715574BC6639F42E0D5D8985307A566D0873EC041C74DA9F51543ED92027EFF7998A3C5D178A8EF9EB52355414E
http://purl.uniprot.org/uniprot/B3KM21
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CA1D5715574BC6639F42E0D5D8985307A566D0873EC041C74DA9F51543ED92027EFF7998A3C5D178A8EF9EB52355414E
http://purl.uniprot.org/uniprot/#_B3KM21-mappedCitation-22678713
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CA1D5715574BC6639F42E0D5D8985307A566D0873EC041C74DA9F51543ED92027EFF7998A3C5D178A8EF9EB52355414E