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DESCRIBE <http://purl.uniprot.org/SHA-384/DB013DBC2D1D8D0C5936F224D01AF0837930B2DF5172CA95AA36CDCBCBCDD404E2E03E1ADE10B1654F36B7AFF51B881A>
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http://purl.uniprot.org/SHA-384/DB013DBC2D1D8D0C5936F224D01AF0837930B2DF5172CA95AA36CDCBCBCDD404E2E03E1ADE10B1654F36B7AFF51B881A
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/DB013DBC2D1D8D0C5936F224D01AF0837930B2DF5172CA95AA36CDCBCBCDD404E2E03E1ADE10B1654F36B7AFF51B881A
http://www.w3.org/2000/01/rdf-schema#comment
"NR5A1 gene mutations are a relatively frequent cause of 46 XY disorders of sex development in humans."
xsd:string
http://purl.uniprot.org/uniprot/#_E9F9F43B675327F9B8FAF748A0C8CE480AC52E19D09E07FCC07BD3B541F3C93740DB041B2F7CBD0D039CF9B498A2D0E3
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/DB013DBC2D1D8D0C5936F224D01AF0837930B2DF5172CA95AA36CDCBCBCDD404E2E03E1ADE10B1654F36B7AFF51B881A
http://purl.uniprot.org/uniprot/F1DAM0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DB013DBC2D1D8D0C5936F224D01AF0837930B2DF5172CA95AA36CDCBCBCDD404E2E03E1ADE10B1654F36B7AFF51B881A
http://purl.uniprot.org/uniprot/#_F1DAM0-mappedCitation-24434652
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/DB013DBC2D1D8D0C5936F224D01AF0837930B2DF5172CA95AA36CDCBCBCDD404E2E03E1ADE10B1654F36B7AFF51B881A