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DESCRIBE <http://purl.uniprot.org/SHA-384/F76E1F710B6E934A3B33BCD949D18C1B17CBDC7D6C98B5F4AFD4293BE5504CBEF29D18B92B85D054D8C2D93477F63145>
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http://purl.uniprot.org/SHA-384/F76E1F710B6E934A3B33BCD949D18C1B17CBDC7D6C98B5F4AFD4293BE5504CBEF29D18B92B85D054D8C2D93477F63145
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/F76E1F710B6E934A3B33BCD949D18C1B17CBDC7D6C98B5F4AFD4293BE5504CBEF29D18B92B85D054D8C2D93477F63145
http://www.w3.org/2000/01/rdf-schema#comment
"Mutations in MLH1 MSH2 and MSH6 are associated with Lynch syndrome."
xsd:string
http://purl.uniprot.org/uniprot/#_CE74E91E22CDC9C87F9008AE501816A847E591AB1F4E862B033F3CAA7DA14EA7219D6580A0F5007840777F6AFA9C3B38
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/F76E1F710B6E934A3B33BCD949D18C1B17CBDC7D6C98B5F4AFD4293BE5504CBEF29D18B92B85D054D8C2D93477F63145
http://purl.uniprot.org/uniprot/A8W2J0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F76E1F710B6E934A3B33BCD949D18C1B17CBDC7D6C98B5F4AFD4293BE5504CBEF29D18B92B85D054D8C2D93477F63145
http://purl.uniprot.org/uniprot/#_A8W2J0-mappedCitation-21721000
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/F76E1F710B6E934A3B33BCD949D18C1B17CBDC7D6C98B5F4AFD4293BE5504CBEF29D18B92B85D054D8C2D93477F63145