@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk> .
@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:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_head {
  this: np:hasAssertion dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion ;
    np:hasProvenance dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_provenance ;
    np:hasPublicationInfo dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion a np:Assertion .
  dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_provenance a np:Provenance .
  dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion {
  miriam-gene:8170 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGN517236630313a2925ca8f0a8c48b5075 sio:SIO_000628 miriam-gene:8170 , lld:C0003873 ;
    a sio:SIO_001121 .
}
dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_provenance {
  dgn-np:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_assertion dcterms:description "[To determine whether non-missense genetic polymorphisms located in regulatory region of TLR4 are related to RA in a Chinese Han population, four single nucleotide polymorphisms (SNPs) situated on 3' untranslating region (UTR) and 5' UTR were genotyped in 213 RA patients and 247 unrelated ethnically matched controls using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and direct sequencing techniques.]. 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:23129427 ;
    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:NP673788.RA0V-jBg5aZb-9pRJtwqQT8jqPS_9X6y7-ZTrNcmHhukk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:46+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" .
}