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• https://identifiers.org/ensembl/ENSG00000103319
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/Complex/a112b
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/Complex/a282c
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/Complex/a390a
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/Complex/b9fc3
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/Complex/ca85c
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/Complex/f2854
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/ComplexBinding/a112b
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/ComplexBinding/a282c
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/ComplexBinding/a390a
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/ComplexBinding/b9fc3
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/ComplexBinding/ca85c
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/ComplexBinding/f2854
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/a221e
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/a2c1d
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/a3d83
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/ae755
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/b643a
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/bc250
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/bc714
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/bcae2
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/c0a08
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/c11a0
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/c3372
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/caae3
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• http://rdf.wikipathways.org/Pathway/WP5510_r136508/WP/Interaction/e655f
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  • http://purl.org/dc/terms/isPartOf
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• https://identifiers.org/wikipathways/WP5510
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  • http://purl.org/dc/elements/1.1/title
    • 16p12.2 copy number variation syndrome (520kb)
  • http://purl.org/dc/terms/description
    • Copy number variations in the region 16p12.2 (exact position on the chromosome: Chr16:21950135-22431889 (GRCh37), are rare, pathological mutations in the human genome. It is a risk variation for neuropsychiatric diseases like schizophrenia (Kirov et al. 2014, 10.1016/j.biopsych.2013.07.022)
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  • http://vocabularies.wikipathways.org/wp#organismName
    • Homo sapiens
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• https://identifiers.org/ensembl/ENSG00000198793
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