@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww> .
@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:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_head {
  this: np:hasAssertion dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion ;
    np:hasProvenance dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_provenance ;
    np:hasPublicationInfo dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion a np:Assertion .
  dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_provenance a np:Provenance .
  dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  lld:C0011570 a ncit:C7057 .
  dgn-gda:DGNa065ba824733719e3b7389faf88e3ba4 sio:SIO_000628 miriam-gene:1813 , lld:C0011570 ;
    a sio:SIO_001121 .
}
dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_provenance {
  dgn-np:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_assertion dcterms:description "[Because the D2 dopamine receptor (DRD2) A1 allele has been associated with alcoholism and other substance use disorders, negative affect, measured by the Beck Depression Inventory (BDI), was determined in four groups of children: boys and girls with the A1+ allele (A1A1 and A1A2 genotypes) and with the A1- allele (A2A2 genotype).]. 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:13679114 ;
    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:NP555544.RA0N3XYUtfqZa3qWhQfCuogC6C1nZ_D1pOmKvjL6WzWww130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}