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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idad0490d4
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idb69880c2
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idbbe02e53
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idbc2c3e40
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idbc729a93
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idcc78219
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idd36728f8
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/ide3bc70dd
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/ide6e0e29f
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/ideef7d437
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idf20e8561
  • http://purl.org/dc/terms/isPartOf
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• http://rdf.wikipathways.org/Pathway/WP5348_r138774/WP/Interaction/idf45f799
  • http://purl.org/dc/terms/isPartOf
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• https://identifiers.org/wikipathways/WP5348_r138774
  • http://www.w3.org/1999/02/22-rdf-syntax-ns#type
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    • http://www.w3.org/2004/02/skos/core#Collection
  • http://xmlns.com/foaf/0.1/page
    • http://www.wikipathways.org/instance/WP5348_r138774
  • 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
    • 11p11.2 copy number variation syndrome
  • http://purl.org/dc/terms/description
    • The molecular pathways of genes located at the region 11p11.2. A deletion in 11p11.2 can cause the Potocki-Shaffer syndrome (MIM # 601224) which is characterised by malformations in the heart, kidney and urinary tract. The chromosomal location was taken from Kirov et al. 2014 and literature cited there (chr11:43940000-46020000, GRCh37).
  • http://purl.org/dc/terms/identifier
    • WP5348
  • http://purl.org/spar/cito/cites
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    • https://identifiers.org/pubmed/10602019
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    • https://identifiers.org/pubmed/15661757
    • https://identifiers.org/pubmed/19587235
    • https://identifiers.org/pubmed/15205336
    • https://identifiers.org/pubmed/15492270
  • http://vocabularies.wikipathways.org/wp#diseaseOntologyTag
    • http://purl.obolibrary.org/obo/DOID_0111687
  • http://vocabularies.wikipathways.org/wp#isAbout
    • http://rdf.wikipathways.org/Pathway/WP5348_r138774
  • http://vocabularies.wikipathways.org/wp#ontologyTag
    • http://purl.obolibrary.org/obo/PW_0000013
    • http://vocabularies.wikipathways.org/wp#Curation:Diseases
    • http://purl.obolibrary.org/obo/DOID_0111687
    • http://vocabularies.wikipathways.org/wp#Curation:ONTOX
    • http://vocabularies.wikipathways.org/wp#Curation:AnalysisCollection
    • 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
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