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DESCRIBE <http://purl.uniprot.org/SHA-384/86BA0C54C53C4F9E662FFEFB687479BD1BEE4D5BACFAE3EF29A5C91838A9C440A7D2DC1927A4BFE2F826779146E5A825>
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http://purl.uniprot.org/SHA-384/86BA0C54C53C4F9E662FFEFB687479BD1BEE4D5BACFAE3EF29A5C91838A9C440A7D2DC1927A4BFE2F826779146E5A825
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/86BA0C54C53C4F9E662FFEFB687479BD1BEE4D5BACFAE3EF29A5C91838A9C440A7D2DC1927A4BFE2F826779146E5A825
http://www.w3.org/2000/01/rdf-schema#comment
"Data suggested that the p.C634Y/V292M/R67H/R982C mutation exhibited an aggressive phenotype while p.V292M/R67H/R982C presented a milder pathogenicity of MTC and likely predisposed to familial medullary thyroid carcinoma."
xsd:string
http://purl.uniprot.org/uniprot/#_48B9701C915131D70C0800299FEA277E5BEDE714E02BA56267BAF2EBAD6FEDA1542D575FB71D27D3CEFE513A73FB37EA
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/86BA0C54C53C4F9E662FFEFB687479BD1BEE4D5BACFAE3EF29A5C91838A9C440A7D2DC1927A4BFE2F826779146E5A825
http://purl.uniprot.org/uniprot/P07949
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/86BA0C54C53C4F9E662FFEFB687479BD1BEE4D5BACFAE3EF29A5C91838A9C440A7D2DC1927A4BFE2F826779146E5A825
http://purl.uniprot.org/uniprot/#_P07949-mappedCitation-21655256
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/86BA0C54C53C4F9E662FFEFB687479BD1BEE4D5BACFAE3EF29A5C91838A9C440A7D2DC1927A4BFE2F826779146E5A825