@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0> .
@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:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_head {
  this: np:hasAssertion dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_assertion ;
    np:hasProvenance dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_provenance ;
    np:hasPublicationInfo dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_assertion a np:Assertion .
  dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_provenance a np:Provenance .
  dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_assertion {
  miriam-gene:4153 a ncit:C16612 .
  lld:C0745287 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_provenance {
  dgn-np:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_assertion dcterms:description "[We selected nine genetic variations in four genes involved in immune response modulation (CCR5, TLR2, TLR4 and MBL2) and assessed their association with tubal factor infertility by comparing genotype frequencies among 163 women with tubal factor infertility and 400 control individuals.]. 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:20598754 ;
    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:NP556776.RAbA6DMQKlx3Aqsw92MDK3UMRjshYNwRvGnWGvFePu9x0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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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}