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    • http://www.w3.org/2004/02/skos/core#Collection
    • http://vocabularies.wikipathways.org/wp#Pathway
  • http://xmlns.com/foaf/0.1/page
    • http://www.wikipathways.org/instance/WP5352_r128797
  • http://purl.org/dc/elements/1.1/identifier
    • https://identifiers.org/wikipathways/WP5352
  • http://purl.org/dc/elements/1.1/source
    • WikiPathways
  • http://purl.org/dc/elements/1.1/title
    • 10q11.21q11.23 copy number variation syndrome
  • http://purl.org/dc/terms/description
    • 10q11.21q11.23 copy number variation (CNV) syndrome is a rare genetic disorder caused by a deletion or duplication of genetic material on chromosome 10. The exact genetic location chr10:49,390,199-51,058,796 (GRCh37) was taken from Kirov et al. 2014 and literature cited there.
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    • WP5352
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    • https://identifiers.org/pubmed/22466612
    • https://identifiers.org/pubmed/21398629
    • https://identifiers.org/pubmed/19706687
  • http://vocabularies.wikipathways.org/wp#isAbout
    • http://rdf.wikipathways.org/Pathway/WP5352_r128797
  • http://vocabularies.wikipathways.org/wp#ontologyTag
    • http://vocabularies.wikipathways.org/wp#Curation:Diseases
    • http://purl.obolibrary.org/obo/PW_0000013
    • http://vocabularies.wikipathways.org/wp#Curation:RareDiseases
    • http://vocabularies.wikipathways.org/wp#Curation:AnalysisCollection
  • http://vocabularies.wikipathways.org/wp#organism
    • http://purl.obolibrary.org/obo/NCBITaxon_9606
  • http://vocabularies.wikipathways.org/wp#organismName
    • Homo sapiens
  • http://vocabularies.wikipathways.org/wp#pathwayOntologyTag
    • http://purl.obolibrary.org/obo/PW_0000013
  • http://xmlns.com/foaf/0.1/img
    • https://www.wikipathways.org//wpi/wpi.php?action=downloadFile&type=svg&pwTitle=Pathway:WP5352&oldid=128797
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    • https://identifiers.org/wikipathways/WP5352_r128797
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    • https://identifiers.org/wikipathways/WP5352_r128797
• https://identifiers.org/ensembl/ENSG00000183691
  • http://purl.org/dc/terms/isPartOf
    • https://identifiers.org/wikipathways/WP5352_r128797
• https://identifiers.org/wikipathways/WP1866
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    • https://identifiers.org/wikipathways/WP5352_r128797
• https://identifiers.org/ensembl/ENSG00000132382
  • http://purl.org/dc/terms/isPartOf
    • https://identifiers.org/wikipathways/WP5352_r128797
• https://identifiers.org/ensembl/ENSG00000166266
  • http://purl.org/dc/terms/isPartOf
    • https://identifiers.org/wikipathways/WP5352_r128797
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    • https://identifiers.org/wikipathways/WP5352_r128797
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