@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8> .
@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:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_head {
  this: np:hasAssertion dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_assertion;
    np:hasProvenance dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_provenance;
    np:hasPublicationInfo dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_assertion a np:Assertion .
  
  dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_provenance a np:Provenance .
  
  dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_assertion {
  miriam-gene:11122 a ncit:C16612 .
  
  lld:C0001973 a ncit:C7057 .
  
  dgn-gda:DGN3df31920178a457b5f7047af12592f2e sio:SIO_000628 miriam-gene:11122, lld:C0001973;
    a sio:SIO_001122 .
}

dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_provenance {
  dgn-np:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_assertion dct:description
      "[These data, coupled with cell and animal model data implicating neuronal signaling in alcohol response, support the conclusion that neuronal signaling is mechanistically involved in alcohols cellular and behavioral effects. Further, these data suggest that genetic variation in these signaling pathways contribute to human variation in alcohol response. Finally, this concordance of the cell, animal, and human findings supports neuronal signaling, particularly glutamate signaling, as a prime target for translational studies to understand and eventually modulate alcohols effects.]. 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:20201926;
    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:NP83016.RAyD2C-c150sBe_OOfyABGNHhpn21I1y_n59KWjQesVr8130_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" .
}