@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI> .
@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:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_head {
  this: np:hasAssertion dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion;
    np:hasProvenance dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_provenance;
    np:hasPublicationInfo dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion a np:Assertion .
  
  dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_provenance a np:Provenance .
  
  dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion {
  miriam-gene:4988 a ncit:C16612 .
  
  lld:C0038580 a ncit:C7057 .
  
  dgn-gda:DGN9b4ecfa713dbee2cfcaa4aca2c448624 sio:SIO_000628 miriam-gene:4988, lld:C0038580;
    a sio:SIO_001121 .
}

dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_provenance {
  dgn-np:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_assertion dcterms:description
      "[Previous studies of the association of the C17T polymorphism of the mu opiate receptor gene with substance dependence compared cases with substance dependence to controls and usually found no significant association.]. 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:21070507;
    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:NP223692.RAdWaLpS3afiSqTBsEEPtQ7IVnxylZ1o-94RqRUOsU3OI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:04+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" .
}