@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY> .
@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:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_head {
  this: np:hasAssertion dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_assertion;
    np:hasProvenance dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_provenance;
    np:hasPublicationInfo dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_provenance a np:Provenance .
  
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      np:PublicationInfo .
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dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_assertion {
  miriam-gene:255239 a ncit:C16612 .
  
  lld:C1839238 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_provenance {
  dgn-np:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_assertion dcterms:description
      "[The two objectives of this study were (1) to replicate the previous finding that a single nucleotide polymorphism (SNP) in the ANKK1 gene (SNP rs1800497 formerly known as the DRD2 TAQ1 A allele) is associated with measures of learning and response latency after traumatic brain injury (TBI) and (2) to further characterize the genetic basis of the effect by testing the strength of association and degree of linkage disequilibrium between the cognitive outcome measures and a selected ensemble of 31 polymorphisms from three adjacent genes in the region of rs1800497.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    prov:wasDerivedFrom dgn-void:befree-20140225;
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  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:NP259873.RAV5PjGkkMAJ46BRgJVqFzsKHRYjLkaAQCdmNgF60A_nY130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    prv:usedData dgn-void:disgenetrdf;
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