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DESCRIBE <http://purl.uniprot.org/SHA-384/E927F1DA3073452723450E6BDDB6030A6473B20E70D11661A49D11B0C63E48C8B4CA510C9F4E4E3880A1A3CA10410D48>
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http://purl.uniprot.org/SHA-384/E927F1DA3073452723450E6BDDB6030A6473B20E70D11661A49D11B0C63E48C8B4CA510C9F4E4E3880A1A3CA10410D48
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/E927F1DA3073452723450E6BDDB6030A6473B20E70D11661A49D11B0C63E48C8B4CA510C9F4E4E3880A1A3CA10410D48
http://www.w3.org/2000/01/rdf-schema#comment
"Sequencing analysis of the complete coding region of CDKN1B in a panel of premature ovarian failure patients and control subjects reveals a novel mutation potentially related to the phenotype."
xsd:string
http://purl.uniprot.org/uniprot/#_11A41C629958A80ADEA42C49214457F519DD767FEDA3F4AB19BA2B0E66B76D49899F91C6B5C61439F352391DC6FDC276
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/E927F1DA3073452723450E6BDDB6030A6473B20E70D11661A49D11B0C63E48C8B4CA510C9F4E4E3880A1A3CA10410D48
http://purl.uniprot.org/uniprot/Q96TE0
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E927F1DA3073452723450E6BDDB6030A6473B20E70D11661A49D11B0C63E48C8B4CA510C9F4E4E3880A1A3CA10410D48
http://purl.uniprot.org/uniprot/#_Q96TE0-mappedCitation-21575944
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/E927F1DA3073452723450E6BDDB6030A6473B20E70D11661A49D11B0C63E48C8B4CA510C9F4E4E3880A1A3CA10410D48