@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4> .
@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:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_head {
  this: np:hasAssertion dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_assertion;
    np:hasProvenance dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_provenance;
    np:hasPublicationInfo dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_assertion a np:Assertion .
  
  dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_provenance a np:Provenance .
  
  dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C0016034 a ncit:C7057 .
  
  dgn-gda:DGNe95f86ce9c94fc0cf8df8ffbbebe5ecc sio:SIO_000628 miriam-gene:1545, lld:C0016034;
    a sio:SIO_001121 .
}

dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_provenance {
  dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_assertion dcterms:description
      "[Odds ratios and 95% confidence intervals (in parentheses) for the midpoints of the first, second, fourth, and fifth quintiles of gene expression levels compared with the overall median levels in BBD subjects were 0.21 (0.07-0.67), 0.81 (0.69-0.95), 1.20 (1.05-1.38), and 1.55 (1.12-2.15) for CYP1B1 and 1.72 (1.17-2.55), 1.19 (1.05-1.35), 0.83 (0.73-0.95), and 0.78 (0.65-0.93) for COMT, respectively.]. 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:17507616;
    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 .
}

dgn-np:NP932078.RAtxhEkWGFIwVSG0FMTso3X_xFESM4z-hjv10rvRBpJW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:31+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" .
}