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DESCRIBE <http://purl.uniprot.org/SHA-384/B93446273CC41AA8D0DFA8BC9DB7805F5DFB3DF820706AD0E64A6806F16B3BFBB43FB54E62D5B80BCF338A45812CB4C8>
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http://purl.uniprot.org/SHA-384/B93446273CC41AA8D0DFA8BC9DB7805F5DFB3DF820706AD0E64A6806F16B3BFBB43FB54E62D5B80BCF338A45812CB4C8
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B93446273CC41AA8D0DFA8BC9DB7805F5DFB3DF820706AD0E64A6806F16B3BFBB43FB54E62D5B80BCF338A45812CB4C8
http://www.w3.org/2000/01/rdf-schema#comment
"Whole-exome sequencing in ASD patients from each family identified a second rare inherited genetic variant affecting either the ANK3 genes encoding NLGN4X interacting proteins expressed in inhibitory or in excitatory synapses."
xsd:string
http://purl.uniprot.org/uniprot/#_99A8BFC4EAA8E3D9411750A8C3E545F7FBB220B9818D48778A19F8FF3B94817923B10CDA00F40A294520E13ADFCFE2C4
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B93446273CC41AA8D0DFA8BC9DB7805F5DFB3DF820706AD0E64A6806F16B3BFBB43FB54E62D5B80BCF338A45812CB4C8
http://purl.uniprot.org/uniprot/Q6ZT73
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B93446273CC41AA8D0DFA8BC9DB7805F5DFB3DF820706AD0E64A6806F16B3BFBB43FB54E62D5B80BCF338A45812CB4C8
http://purl.uniprot.org/uniprot/#_Q6ZT73-mappedCitation-26055424
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B93446273CC41AA8D0DFA8BC9DB7805F5DFB3DF820706AD0E64A6806F16B3BFBB43FB54E62D5B80BCF338A45812CB4C8