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• https://identifiers.org/wikipathways/WP4950_r128400
  • http://www.w3.org/1999/02/22-rdf-syntax-ns#type
    • http://vocabularies.wikipathways.org/wp#Pathway
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  • http://xmlns.com/foaf/0.1/page
    • http://www.wikipathways.org/instance/WP4950_r128400
  • http://purl.org/dc/elements/1.1/identifier
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  • http://purl.org/dc/elements/1.1/source
    • WikiPathways
  • http://purl.org/dc/elements/1.1/title
    • 16p11.2 distal deletion syndrome
  • http://purl.org/dc/terms/description
    • 16p11.2 distal deletion syndrome is a rare genetic disorder (copy number variation) caused by a deletion on chromosome 16 in the range 28.74-28.95-Mb. The breakpoints in this pathway are chr16:28,823,196-29,046,783 (GHCh37) from Kendall et al. 2017 https://doi.org/10.1016/j.biopsych.2016.08.014.
  • http://purl.org/dc/terms/identifier
    • WP4950
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  • http://vocabularies.wikipathways.org/wp#diseaseOntologyTag
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    • http://purl.obolibrary.org/obo/DOID_0060398
  • http://vocabularies.wikipathways.org/wp#isAbout
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  • http://vocabularies.wikipathways.org/wp#ontologyTag
    • http://purl.obolibrary.org/obo/DOID_630
    • http://purl.obolibrary.org/obo/PW_0000013
    • http://vocabularies.wikipathways.org/wp#Curation:AnalysisCollection
    • http://vocabularies.wikipathways.org/wp#Curation:ONTOX
    • http://purl.obolibrary.org/obo/DOID_0060398
    • http://vocabularies.wikipathways.org/wp#Curation:RareDiseases
  • 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
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