@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik> .
@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:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_head {
  this: np:hasAssertion dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_assertion;
    np:hasProvenance dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_provenance;
    np:hasPublicationInfo dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_assertion a np:Assertion .
  
  dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_provenance a np:Provenance .
  
  dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_assertion {
  miriam-gene:2736 a ncit:C16612 .
  
  lld:C0152115 a ncit:C7057 .
  
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dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_provenance {
  dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_assertion dcterms:description
      "[Moreover, the application of the genome-wide association study (GWAS) to the susceptibility of TD has revealed certain associated genes that previously were never considered to be associated with TD, such as the rs7669317 on 4q24, GLI2 gene, GABA pathway genes, and HSPG2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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 .
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dgn-np:NP690399.RAGKP9Lqu75IMH2FHSo8GecPpULja9jfVNRdVOSd32Eik130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:59+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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