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DESCRIBE <http://purl.uniprot.org/SHA-384/07E8F3AB55AF94A96C19A34E410CB0EF5071E19D14ECC6F7E06DBC2AC80D840CA60EB4B658AA9120E386424C76173218>
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http://purl.uniprot.org/SHA-384/07E8F3AB55AF94A96C19A34E410CB0EF5071E19D14ECC6F7E06DBC2AC80D840CA60EB4B658AA9120E386424C76173218
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/07E8F3AB55AF94A96C19A34E410CB0EF5071E19D14ECC6F7E06DBC2AC80D840CA60EB4B658AA9120E386424C76173218
http://www.w3.org/2000/01/rdf-schema#comment
"Neurodevelopmental disorder with microcephaly hypotonia and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene."
xsd:string
http://purl.uniprot.org/uniprot/#_09C85CE1EF1B29C9D421ABA1CED24FD6006C5001C046C97BE4125D9610B52A25858F47257B0817149A1D7CE88562E469
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/07E8F3AB55AF94A96C19A34E410CB0EF5071E19D14ECC6F7E06DBC2AC80D840CA60EB4B658AA9120E386424C76173218
http://purl.uniprot.org/uniprot/B7ZB72
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/07E8F3AB55AF94A96C19A34E410CB0EF5071E19D14ECC6F7E06DBC2AC80D840CA60EB4B658AA9120E386424C76173218
http://purl.uniprot.org/uniprot/#_B7ZB72-mappedCitation-35379233
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/07E8F3AB55AF94A96C19A34E410CB0EF5071E19D14ECC6F7E06DBC2AC80D840CA60EB4B658AA9120E386424C76173218