@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI> .
@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 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:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_head {
  this: np:hasAssertion dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_assertion;
    np:hasProvenance dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_provenance;
    np:hasPublicationInfo dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_assertion a np:Assertion .
  
  dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_provenance a np:Provenance .
  
  dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_assertion {
  miriam-gene:4886 a ncit:C16612 .
  
  lld:C0236733 a ncit:C7057 .
  
  dgn-gda:DGNb62349c49043969729f5d0e0fdfebee8 sio:SIO_000628 miriam-gene:4886, lld:C0236733;
    a sio:SIO_001122 .
}

dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_provenance {
  dgn-np:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_assertion dct:description
      "[It is possible that genetic variants of the NPY1R gene affect the NPY-NPY receptor type Y1 signaling system in the brain, which may result in susceptibility to methamphetamine dependence or the development of methamphetamine psychosis, but the present findings need to be confirmed on replication.]. 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:19566775;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP83773.RA1JgrQX9wpXb67nNYLC_JzaUlam9wKuC5PTaIPLTdAxI130_publicationInfo {
  this: dct:created "2014-10-02T12:32:41+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}