@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE> .
@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:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_head {
   this: np:hasAssertion dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_assertion ;
    np:hasProvenance dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_provenance ;
    np:hasPublicationInfo dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_assertion a np:Assertion .
  dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_provenance a np:Provenance .
  dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_assertion {
   miriam-gene:1312 a ncit:C16612 .
  lld:C0033975 a ncit:C7057 .
  dgn-gda:DGNa6ebe5343f9ce34a3910aded641887a6 sio:SIO_000628 miriam-gene:1312 , lld:C0033975 ;
    a sio:SIO_001121 .
}
dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_provenance {
   dgn-np:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_assertion dcterms:description "[Linkage between the DRD4 and COMT genes and cognitive measures characterizing verbal memory, executive functions, and associative processes was studied in 150 patients with schizophrenia, 83 of their relatives, and 118 mentally healthy subjects without any family history of psychoses, with the aim of detecting the main effects of the polymorphic markers -809G/A and -521C/T (DRD4) and Val158Met (COMT) when present individually and together.]. 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:17763983 ;
    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:NP240083.RADNS7a3zFwB7wthXhSsxWWRFnu6mDkvUntpUjbLUf9iE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:34:14+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" .
}