@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4> .
@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:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_head {
  this: np:hasAssertion dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion ;
    np:hasProvenance dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_provenance ;
    np:hasPublicationInfo dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion a np:Assertion .
  dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_provenance a np:Provenance .
  dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion {
  miriam-gene:10392 a ncit:C16612 .
  lld:C0014170 a ncit:C7057 .
  dgn-gda:DGN8e60d5bf05b7404fd679b15720eb1a50 sio:SIO_000628 miriam-gene:10392 , lld:C0014170 ;
    a sio:SIO_001122 .
}
dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_provenance {
  dgn-np:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_assertion dcterms:description "[The variant C allele of rs5743836 causes greater TLR9 transcriptional activity compared to the T allele, therefore, higher TLR9 activity may be related to efficient removal of microbial pathogens within the endometrium. Clearly, the association of these TLR9 polymorphisms and endometrial cancer risk must be further examined in an independent population. The results point towards the importance of examining immune response in endometrial tumourigenesis to understand new pathways that may be implicated in disease.]. 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:20646321 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP85562.RAAAZWAf5jXHdvfa2k1dWU91mv9I0TN4a5bff7IBvGZW4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:42+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" .
}