@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew> .
@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:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_head {
   this: np:hasAssertion dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_assertion ;
    np:hasProvenance dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_provenance ;
    np:hasPublicationInfo dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_assertion a np:Assertion .
  dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_provenance a np:Provenance .
  dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_assertion {
   miriam-gene:1813 a ncit:C16612 .
  lld:C0595905 a ncit:C7057 .
  dgn-gda:DGNc9a56f66f5ce93878af1509ddd72b183 sio:SIO_000628 miriam-gene:1813 , lld:C0595905 ;
    a sio:SIO_001121 .
}
dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_provenance {
   dgn-np:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_assertion dcterms:description "[Polymorphisms in the catechol-O-methyltransferase (COMT) and the dopamine D4 receptor (DRD4) genes are likely to impact directly on the functioning of the frontal cortex, whereas polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes might influence frontal cortex functioning indirectly via strong frontostriatal connections.]. 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:20210499 ;
    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:NP326749.RAEm3iBRMWBZVYrUP1AgGMK6YE9U75Pp3yMpB06VZDMew130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:11+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" .
}