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DESCRIBE <http://purl.uniprot.org/SHA-384/C78A14A5EC990687262AA2664064619A8E9A2A30099DED7B53DF900A0858F7ADBF76550B33BE93D4E127D603AFEC12E5>
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http://purl.uniprot.org/SHA-384/C78A14A5EC990687262AA2664064619A8E9A2A30099DED7B53DF900A0858F7ADBF76550B33BE93D4E127D603AFEC12E5
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/C78A14A5EC990687262AA2664064619A8E9A2A30099DED7B53DF900A0858F7ADBF76550B33BE93D4E127D603AFEC12E5
http://www.w3.org/2000/01/rdf-schema#comment
"Te results of this study suggested taht genetic variations in MMEL1 ECE1 ECE2 AGER PLG PLAT NR1H3 MMP3 LRP1 TTR NR1H2 and MMP9 genes do not play major role among the Finnish AD patient cohort."
xsd:string
http://purl.uniprot.org/uniprot/#_ED3BDB57C5FB3A89D80ECD26446B94BBF93B6229C2A9F0EDCA4AC79BD62A8F7B44832AAA866EA7BC48B6174F097A6DEF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/C78A14A5EC990687262AA2664064619A8E9A2A30099DED7B53DF900A0858F7ADBF76550B33BE93D4E127D603AFEC12E5
http://purl.uniprot.org/uniprot/Q495T6
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C78A14A5EC990687262AA2664064619A8E9A2A30099DED7B53DF900A0858F7ADBF76550B33BE93D4E127D603AFEC12E5
http://purl.uniprot.org/uniprot/#_Q495T6-mappedCitation-22027013
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/C78A14A5EC990687262AA2664064619A8E9A2A30099DED7B53DF900A0858F7ADBF76550B33BE93D4E127D603AFEC12E5