@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc> .
@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:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_head {
  this: np:hasAssertion dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion ;
    np:hasProvenance dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_provenance ;
    np:hasPublicationInfo dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion a np:Assertion .
  dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_provenance a np:Provenance .
  dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion {
  miriam-gene:26188 a ncit:C16612 .
  lld:C0003873 a ncit:C7057 .
  dgn-gda:DGN119af3b91427e17b4fcd74e5446f0fad sio:SIO_000628 miriam-gene:26188 , lld:C0003873 ;
    a sio:SIO_001121 .
}
dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_provenance {
  dgn-np:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_assertion dcterms:description "[Among the 120 RA patients being heterozygous in the promoter region of Fas_-670A/G (OR 1.42,CI 0.92-1.52, P = 0.18) and FasL_-844C/T (OR 1.42, CI 0.92-1.52, P = 0.18) and homozygous in the minor allele for FasLIVS2nt_124G/G (OR 1.43, CI 0.76-1.81, P = 0.7), the frequency of these polymorphisms is higher in the cases than in controls and the elevated risk of RA were observed when the patient compared with controls, although this is not statistically significant.]. 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:21879377 ;
    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:NP846184.RA0VpVGjDtNItYG_3Chah-mCzT8U-iTI7XFxmoYe4JNhc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:37+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" .
}