@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY> .
@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:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_head {
  this: np:hasAssertion dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_assertion ;
    np:hasProvenance dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_provenance ;
    np:hasPublicationInfo dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_provenance a np:Provenance .
  dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_assertion {
  miriam-gene:7097 a ncit:C16612 .
  lld:C0024141 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_provenance {
  dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_assertion dcterms:description "[In conclusion, a case-control study was used to analyze, for the first time, the influence of TLR2 and TLR4 gene polymorphism on the predisposition and clinical characteristics of SLE and RA but provided no evidence for association of TLR2 or TLR4 gene polymorphism with either disease in the population under study.]. 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:14651524 ;
    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 ;
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}
dgn-np:NP398304.RAEks-LXE6q7yzrAlF4WXKJYdvCsl1xEaN4gMQUnQAXpY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:57+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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