@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU> .
@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:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_head {
  this: np:hasAssertion dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_assertion ;
    np:hasProvenance dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_provenance ;
    np:hasPublicationInfo dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_assertion a np:Assertion .
  dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_provenance a np:Provenance .
  dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_assertion {
  miriam-gene:7984 a ncit:C16612 .
  lld:C0024141 a ncit:C7057 .
  dgn-gda:DGN47275593a31205a4066cc07dfe68127a sio:SIO_000628 miriam-gene:7984 , lld:C0024141 ;
    a sio:SIO_001121 .
}
dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_provenance {
  dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_assertion dcterms:description "[However, it should be noted that the statistical power of our study is relatively low, which likely did not have adequate power to detect the actual correlation between the selected SNPs and SLE susceptibility; moreover, we cannot discard a possible association of other variants within the region covering TIM with SLE as a genetic risk factor, with larger samples in different populations.]. 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:21367814 ;
    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:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:10+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 ;
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