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DESCRIBE <http://purl.uniprot.org/SHA-384/5195DF1AF6BE1B89A4A8134ECB235BACCEA0D9768209C35B4E53AACDBB471B7BFE41B53C98227039D99FCF8921FA6C28>
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http://purl.uniprot.org/SHA-384/5195DF1AF6BE1B89A4A8134ECB235BACCEA0D9768209C35B4E53AACDBB471B7BFE41B53C98227039D99FCF8921FA6C28
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5195DF1AF6BE1B89A4A8134ECB235BACCEA0D9768209C35B4E53AACDBB471B7BFE41B53C98227039D99FCF8921FA6C28
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of gene-disease association. (HuGE Navigator); 22 MC1R variants were identified in Israeli Jewish individuals two of which (i.e. M73I and 496_497insG) are novel."
xsd:string
http://purl.uniprot.org/uniprot/#_BFF5F911E37896CB7AB956A560B112130A72FA1C125ACB70BBE89F13877F67A29C2E143BA6D88D5635EF45158DB4C9BC
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5195DF1AF6BE1B89A4A8134ECB235BACCEA0D9768209C35B4E53AACDBB471B7BFE41B53C98227039D99FCF8921FA6C28
http://purl.uniprot.org/uniprot/Q6UR92
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5195DF1AF6BE1B89A4A8134ECB235BACCEA0D9768209C35B4E53AACDBB471B7BFE41B53C98227039D99FCF8921FA6C28
http://purl.uniprot.org/uniprot/#_Q6UR92-mappedCitation-19269164
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5195DF1AF6BE1B89A4A8134ECB235BACCEA0D9768209C35B4E53AACDBB471B7BFE41B53C98227039D99FCF8921FA6C28