@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_head {
  this: np:hasAssertion dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_assertion;
    np:hasProvenance dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_provenance;
    np:hasPublicationInfo dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_assertion a np:Assertion .
  
  dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_provenance a np:Provenance .
  
  dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_assertion {
  miriam-gene:1312 a ncit:C16612 .
  
  lld:C1298685 a ncit:C7057 .
  
  dgn-gda:DGN2d790d8f414dd0c57f248706f10a4566 sio:SIO_000628 miriam-gene:1312, lld:C1298685;
    a sio:SIO_001121 .
}

dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_provenance {
  dgn-np:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_assertion dcterms:description
      "[These findings from an experimental model converge with those from a surgical cohort and provide additional evidence that the presence of elevated pain catastrophizing and COMT diplotype indicative of low COMT enzyme activity have the potential to increase the risk of developing chronic pain syndromes.]. 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:18936597;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP698996.RAJKUyRc8RJyfXEko2Agdm1rcMLKB3NpvEw45Un60C8l0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:02+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}