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DESCRIBE <http://purl.uniprot.org/SHA-384/F352BD96DB1B5A7E8F2E9C7C1BBBF6C59D9B27A1A10B08A7BD6E1D1755E5076F170CAE3E42B6E92192235D2C0C842FD9>
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http://purl.uniprot.org/SHA-384/F352BD96DB1B5A7E8F2E9C7C1BBBF6C59D9B27A1A10B08A7BD6E1D1755E5076F170CAE3E42B6E92192235D2C0C842FD9
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F352BD96DB1B5A7E8F2E9C7C1BBBF6C59D9B27A1A10B08A7BD6E1D1755E5076F170CAE3E42B6E92192235D2C0C842FD9
http://www.w3.org/2000/01/rdf-schema#comment
"Results from this study indicate that the 2p25.3 duplication disrupting PXDN and MYT1L is a potential autism-causing variant in the pedigree reported here and should receive further consideration as a candidate for autism"
xsd:string
http://purl.uniprot.org/uniprot/#_20CFD99B9D7922D5EAE40BBDD13012503D4ED17AE15DD55354AB73BF01205E2C9A20D6EBE3C861AD92A85EC510E330CC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F352BD96DB1B5A7E8F2E9C7C1BBBF6C59D9B27A1A10B08A7BD6E1D1755E5076F170CAE3E42B6E92192235D2C0C842FD9
http://purl.uniprot.org/uniprot/Q96GF5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F352BD96DB1B5A7E8F2E9C7C1BBBF6C59D9B27A1A10B08A7BD6E1D1755E5076F170CAE3E42B6E92192235D2C0C842FD9
http://purl.uniprot.org/uniprot/#_Q96GF5-mappedCitation-22157634
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F352BD96DB1B5A7E8F2E9C7C1BBBF6C59D9B27A1A10B08A7BD6E1D1755E5076F170CAE3E42B6E92192235D2C0C842FD9