@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY> .
@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:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_head {
  this: np:hasAssertion dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion;
    np:hasProvenance dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance;
    np:hasPublicationInfo dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion a np:Assertion .
  
  dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance a np:Provenance .
  
  dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion {
  miriam-gene:414 a ncit:C16612 .
  
  lld:C0012236 a ncit:C7057 .
  
  dgn-gda:DGN145787213aaaf9c999bc3a1b30f9a1b9 sio:SIO_000628 miriam-gene:414, lld:C0012236;
    a sio:SIO_001121 .
}

dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_provenance {
  dgn-np:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_assertion dcterms:description
      "[As autistic symptoms are increased in individuals with 22q11.2 deletion syndrome, and large 22q11.2 deletions and duplications have been observed in ASD individuals, in this study, 98 individuals with ASD and 234 control individuals were genotyped for eight single-nucleotide polymorphisms in ADORA2A.]. 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:19565319;
    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:NP748252.RAzLE8no3PSWQnM4nNpCXLZEGwAOpvr1eZxSES2Fi8WZY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:24+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" .
}