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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/617DBB9E2C55C16433206DF12EBE7C7E74C7993FE35808FACDF96C3FA75DB788F361660023E52740402BCACE53E256AF>
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http://purl.uniprot.org/SHA-384/617DBB9E2C55C16433206DF12EBE7C7E74C7993FE35808FACDF96C3FA75DB788F361660023E52740402BCACE53E256AF
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/617DBB9E2C55C16433206DF12EBE7C7E74C7993FE35808FACDF96C3FA75DB788F361660023E52740402BCACE53E256AF
http://www.w3.org/2000/01/rdf-schema#comment
"common DNA variants in TBX1 may be nominally causative for CP in patients with 22q11DS. This raises the possibility that genes elsewhere on the remaining allele of 22q11.2 or in the genome could be relevant."
xsd:string
http://purl.uniprot.org/uniprot/#_042D5D1E2B3B8DD2B9AC749908F8AC3D306C25EE879D69401BDDAA753BD81A759A84750CCC9D07357D7B9F43FBFCB046
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/617DBB9E2C55C16433206DF12EBE7C7E74C7993FE35808FACDF96C3FA75DB788F361660023E52740402BCACE53E256AF
http://purl.uniprot.org/uniprot/Q152R5
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/617DBB9E2C55C16433206DF12EBE7C7E74C7993FE35808FACDF96C3FA75DB788F361660023E52740402BCACE53E256AF
http://purl.uniprot.org/uniprot/#_Q152R5-mappedCitation-23034814
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/617DBB9E2C55C16433206DF12EBE7C7E74C7993FE35808FACDF96C3FA75DB788F361660023E52740402BCACE53E256AF