@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto> .
@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:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_head {
  this: np:hasAssertion dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion ;
    np:hasProvenance dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_provenance ;
    np:hasPublicationInfo dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion a np:Assertion .
  dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_provenance a np:Provenance .
  dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  lld:C0149654 a ncit:C7057 .
  dgn-gda:DGN07f71c3e406bebef2e3a06d61adbb9a1 sio:SIO_000628 miriam-gene:1813 , lld:C0149654 ;
    a sio:SIO_001121 .
}
dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_provenance {
  dgn-np:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_assertion dcterms:description "[Further, interaction effects were found between the DRD2 TaqIA polymorphism and conduct disorder (trend level) as well as A1+ status and impulsivity, such that adolescents who were carriers of the A1 allele, and had conduct disorder or impulsive behavior, reported higher levels of problematic alcohol use than those who were non-carriers (A2/A2 or A1-).]. 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:19344737 ;
    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:NP477320.RAYwy7AkrZMQbCykbCHRTCbCc3BBTalB1BDF7W_irCgto130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:46+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" .
}