@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g> .
@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:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_head {
  this: np:hasAssertion dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_assertion ;
    np:hasProvenance dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_provenance ;
    np:hasPublicationInfo dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_assertion a np:Assertion .
  dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_provenance a np:Provenance .
  dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_assertion {
  miriam-gene:51324 a ncit:C16612 .
  lld:C0013146 a ncit:C7057 .
  dgn-gda:DGNda24bfccebfdcc70697e4dbd6148b02b sio:SIO_000628 miriam-gene:51324 , lld:C0013146 ;
    a sio:SIO_001121 .
}
dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_provenance {
  dgn-np:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_assertion dcterms:description "[To examine the hypothesis that individuals carrying the Gts gene are at increased risk to develop alcohol use problems, the same TS (Tourette Syndrome) and ADHD probands, relatives and controls used in the prior study of drug abuse were also studied using a structured questionnaire based on the Diagnostic Interview Schedule and the MAST test.]. 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:8082551 ;
    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:NP338867.RAR8C0gZRN7Z6_MFLh7TTfnU5OF3qcqd9i_ttGhdOHV5g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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> ;
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}