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DESCRIBE <http://purl.uniprot.org/SHA-384/CF2212E3E6C30CCA3E6DEB6A356884C4896077E00C0158535C781E51A57BAA4E172D914C8CDA3FE025E7BB95EFC153AE>
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http://purl.uniprot.org/SHA-384/CF2212E3E6C30CCA3E6DEB6A356884C4896077E00C0158535C781E51A57BAA4E172D914C8CDA3FE025E7BB95EFC153AE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/CF2212E3E6C30CCA3E6DEB6A356884C4896077E00C0158535C781E51A57BAA4E172D914C8CDA3FE025E7BB95EFC153AE
http://www.w3.org/2000/01/rdf-schema#comment
"The phenotype found in the microdeletions of alpha exons of the NRXN1 gene is clearly distinguishable from the one found in the microdeletions of beta exons with macrocephaly epilepsy and mental retardation."
xsd:string
http://purl.uniprot.org/uniprot/#_EAE729AB7307938F6A993311C6598769DCF2B4870F92A8AE5EADCF9C4635F3209C63623B4C2FCCC9B38B2E1EC7327FFF
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/CF2212E3E6C30CCA3E6DEB6A356884C4896077E00C0158535C781E51A57BAA4E172D914C8CDA3FE025E7BB95EFC153AE
http://purl.uniprot.org/uniprot/A0A0D9SEQ7
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CF2212E3E6C30CCA3E6DEB6A356884C4896077E00C0158535C781E51A57BAA4E172D914C8CDA3FE025E7BB95EFC153AE
http://purl.uniprot.org/uniprot/#_A0A0D9SEQ7-mappedCitation-25710691
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/CF2212E3E6C30CCA3E6DEB6A356884C4896077E00C0158535C781E51A57BAA4E172D914C8CDA3FE025E7BB95EFC153AE