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DESCRIBE <http://purl.uniprot.org/SHA-384/B2855EB7C278156B2A22D96C80D620C6B37D409E817D21EFA21AA7C5204F234DA4B53ACE76297EB5023BA4FDCC40F714>
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http://purl.uniprot.org/SHA-384/B2855EB7C278156B2A22D96C80D620C6B37D409E817D21EFA21AA7C5204F234DA4B53ACE76297EB5023BA4FDCC40F714
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B2855EB7C278156B2A22D96C80D620C6B37D409E817D21EFA21AA7C5204F234DA4B53ACE76297EB5023BA4FDCC40F714
http://www.w3.org/2000/01/rdf-schema#comment
"The MTHFR mutation c.677C>T was present in 17.3% of 400 ischemic stroke patients in Sri Lanka. It is the predominant mutation and the only mutation that had patients with the homozygous mutant genotype."
xsd:string
http://purl.uniprot.org/uniprot/#_FBE39C776A27143E8B5A5600C2F2013336346840B6DE08CE11EC981D831C51C6EA988AF570AF2A3E4E2ABE68594D1B37
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B2855EB7C278156B2A22D96C80D620C6B37D409E817D21EFA21AA7C5204F234DA4B53ACE76297EB5023BA4FDCC40F714
http://purl.uniprot.org/uniprot/Q8IU67
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B2855EB7C278156B2A22D96C80D620C6B37D409E817D21EFA21AA7C5204F234DA4B53ACE76297EB5023BA4FDCC40F714
http://purl.uniprot.org/uniprot/#_Q8IU67-mappedCitation-26522268
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B2855EB7C278156B2A22D96C80D620C6B37D409E817D21EFA21AA7C5204F234DA4B53ACE76297EB5023BA4FDCC40F714