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DESCRIBE <http://purl.uniprot.org/SHA-384/5827E40C054149BD2D1E3E1F6B9F8A6432C1B09ECB933F540951CE4B8E94A0983660B98885F29DBEA940339ED0FA7D1F>
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http://purl.uniprot.org/SHA-384/5827E40C054149BD2D1E3E1F6B9F8A6432C1B09ECB933F540951CE4B8E94A0983660B98885F29DBEA940339ED0FA7D1F
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/5827E40C054149BD2D1E3E1F6B9F8A6432C1B09ECB933F540951CE4B8E94A0983660B98885F29DBEA940339ED0FA7D1F
http://www.w3.org/2000/01/rdf-schema#comment
"Exome analysis of Kuwaiti multiple sclerosis patients revealed a missense variant (rs5945430) in Plexin A3 (PLXNA3) gene (Xq28) associated with male-specific MS severity and disability."
xsd:string
http://purl.uniprot.org/uniprot/#_55E496E6ACDE4C76F329B8A2A4EF9BADABAB583E2307A6D3FD85C635F5228D943AC1EE085886788F1D6CD1FB30A581C8
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/5827E40C054149BD2D1E3E1F6B9F8A6432C1B09ECB933F540951CE4B8E94A0983660B98885F29DBEA940339ED0FA7D1F
http://purl.uniprot.org/uniprot/P51805
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5827E40C054149BD2D1E3E1F6B9F8A6432C1B09ECB933F540951CE4B8E94A0983660B98885F29DBEA940339ED0FA7D1F
http://purl.uniprot.org/uniprot/#_P51805-mappedCitation-28536997
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/5827E40C054149BD2D1E3E1F6B9F8A6432C1B09ECB933F540951CE4B8E94A0983660B98885F29DBEA940339ED0FA7D1F