@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4> .
@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:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_head {
  this: np:hasAssertion dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion;
    np:hasProvenance dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_provenance;
    np:hasPublicationInfo dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion a np:Assertion .
  
  dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_provenance a np:Provenance .
  
  dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion {
  miriam-gene:3358 a ncit:C16612 .
  
  lld:C0036341 a ncit:C7057 .
  
  dgn-gda:DGN3bad21d4e52a362ffaaa0ec672b8f9e7 sio:SIO_000628 miriam-gene:3358, lld:C0036341;
    a sio:SIO_001122 .
}

dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_provenance {
  dgn-np:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_assertion dct:description
      "[The D2 polymorphism was found not to be significantly associated with baseline levels or changes in total PANSS in these patients. The D3 genotype is associated with the change in total PANSS (p<0.01), an effect reflecting positive and general (each p<0.0]. 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:15695058;
    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:NP57251.RA-Bcyd8rh8I5SEGQ1VQ4PqCKf-2PmiOW1kj6w_8C0Fy4130_publicationInfo {
  this: dct:created "2014-10-02T12:32:26+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" .
}