@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM> .
@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/v4.0.0/void/> .

dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_head {
  this: np:hasAssertion dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_assertion;
    np:hasProvenance dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_provenance;
    np:hasPublicationInfo dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_assertion a np:Assertion .
  
  dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_provenance a np:Provenance .
  
  dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_assertion {
  miriam-gene:3676 a ncit:C16612 .
  
  lld:C0233715 a ncit:C7057 .
  
  dgn-gda:DGN6c7e33a7a75e0840caf24684cde7c088 sio:SIO_000628 miriam-gene:3676, lld:C0233715;
    a sio:SIO_001121 .
}

dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_provenance {
  dgn-np:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_assertion dcterms:description
      "[The critical region points to a few genes, namely NEUROD1, ZNF804A, PDE1A, and ITGA4, which are good candidates to explain the cognitive and behavioural phenotype, as well as the severe speech impairment associated with the 2q31.2q32.3 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:20552675;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  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:NP819229.RAhitXS-RgN8hSPxPfgHr1y1D5k8V4uQsum-uVNx9bjyM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:56+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}