@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ> .
@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:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_head {
  this: np:hasAssertion dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_assertion;
    np:hasProvenance dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_provenance;
    np:hasPublicationInfo dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_assertion a np:Assertion .
  
  dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_provenance a np:Provenance .
  
  dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C1269683 a ncit:C7057 .
  
  dgn-gda:DGN957baaddfd37ac7ab63c7948a4209bae sio:SIO_000628 miriam-gene:1813, lld:C1269683;
    a sio:SIO_001122 .
}

dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_provenance {
  dgn-np:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_assertion dcterms:description
      "[The results demonstrate that neither polymorphism is associated with P300 amplitude or latency, even after gender analysis. We suggest that these two DRD2 polymorphisms have no major effects on P300 components for the Chinese population. The association between the DRD2 polymorphism and P300 components may depend on ethnicity, the psychiatric state of the subjects, or the investigative paradigms used.]. 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:12422061;
    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:NP45435.RAf1X5mBc_QAErAvlVRWDiki0wRE1z-bE1pxcS3mfGRtQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:20+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" .
}