@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_head {
  this: np:hasAssertion dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_assertion;
    np:hasProvenance dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_provenance;
    np:hasPublicationInfo dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_assertion a np:Assertion .
  
  dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_provenance a np:Provenance .
  
  dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_assertion {
  miriam-gene:150 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN7eec01bc126150f9dd52f887692ddf7a sio:SIO_000628 miriam-gene:150, lld:C0036341;
    a sio:SIO_001121 .
}

dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_provenance {
  dgn-np:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_assertion dcterms:description
      "[With attention directed at the upstream regulatory region of the gene which codes for this receptor (ADRA2A), we proposed that single nucleotide polymorphisms (SNPs) within this region influences susceptibility to schizophrenia by altering the expression of this receptor.]. 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:17034020;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP830020.RAyWmkN21UXdKZvQjSgJeqaV4GQ1BEqvrNjyCwovPB9q0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:28+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}