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Add common prefixes
DESCRIBE <http://purl.uniprot.org/SHA-384/B4D61306E62E0B1497354B928B6FCA83116785535C7CD41D519C6B1C1F27E9F3A2737D661069006CA7E6A399B81B63A7>
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http://purl.uniprot.org/SHA-384/B4D61306E62E0B1497354B928B6FCA83116785535C7CD41D519C6B1C1F27E9F3A2737D661069006CA7E6A399B81B63A7
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/B4D61306E62E0B1497354B928B6FCA83116785535C7CD41D519C6B1C1F27E9F3A2737D661069006CA7E6A399B81B63A7
http://www.w3.org/2000/01/rdf-schema#comment
"Observational study of genotype prevalence. (HuGE Navigator); LRRK2 gene heterozygous mutation (Gly2019 ser) CAUSE dominantly inherited Parkinson's disease."
xsd:string
http://purl.uniprot.org/uniprot/#_1114C5713A4A8437851F0109811B08E96AA760A531288AF2F60207F533AAFCB1BBFCF0F687C5CAB3305441DC014501F4
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/B4D61306E62E0B1497354B928B6FCA83116785535C7CD41D519C6B1C1F27E9F3A2737D661069006CA7E6A399B81B63A7
http://purl.uniprot.org/uniprot/Q17RV3
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B4D61306E62E0B1497354B928B6FCA83116785535C7CD41D519C6B1C1F27E9F3A2737D661069006CA7E6A399B81B63A7
http://purl.uniprot.org/uniprot/#_Q17RV3-mappedCitation-15680457
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/B4D61306E62E0B1497354B928B6FCA83116785535C7CD41D519C6B1C1F27E9F3A2737D661069006CA7E6A399B81B63A7