@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w> .
@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:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_head {
  this: np:hasAssertion dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion ;
    np:hasProvenance dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_provenance ;
    np:hasPublicationInfo dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion a np:Assertion .
  dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_provenance a np:Provenance .
  dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion {
  miriam-gene:3576 a ncit:C16612 .
  lld:C0015672 a ncit:C7057 .
  dgn-gda:DGN42e06e6dd7a61d512eef544a057d52a2 sio:SIO_000628 miriam-gene:3576 , lld:C0015672 ;
    a sio:SIO_001121 .
}
dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_provenance {
  dgn-np:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_assertion dcterms:description "[Logistic regression analyses showed that after controlling for epidemiologic (age and sex), clinical (stage of disease, comorbidities), and symptom (depressed mood and fatigue) variables known to influence pain severity, variant alleles in IL-8 -251T/A [odds ratio (OR), 2.35; 95% confidence interval (95% CI), 1.10-5.03; P = 0.03] persisted as a significant factor for severe pain for White patients.]. 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:18086782 ;
    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:NP236724.RAuO8otX4PNC0vpXEQtLzl09vxtBNcxoLVUNhEeMhev5w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}