@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_head {
  this: np:hasAssertion dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_assertion;
    np:hasProvenance dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_provenance;
    np:hasPublicationInfo dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_publicationInfo;
    a np:Nanopublication .
  
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dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_assertion {
  miriam-gene:79813 a ncit:C16612 .
  
  lld:C0004936 a ncit:C7057 .
  
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dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_provenance {
  dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_assertion dcterms:description
      "[We sequenced BCAs in patients with autism or related NDDs, revealing disruption of 33 loci in four general categories: (1) genes previously associated with abnormal neurodevelopment (e.g., AUTS2, FOXP1, and CDKL5), (2) single-gene contributors to microdeletion syndromes (MBD5, SATB2, EHMT1, and SNURF-SNRPN), (3) novel risk loci (e.g., CHD8, KIRREL3, and ZNF507), and (4) genes associated with later-onset psychiatric disorders (e.g., TCF4, ZNF804A, PDE10A, GRIN2B, and ANK3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP946208.RAg1e7ul7RwKFRLsMPe2BCooom_cH3JkN7BdYqjRHOQ10130_publicationInfo {
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    prv:usedData dgn-void:disgenetv3.0rdf;
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}