@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE> .
@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:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_head {
  this: np:hasAssertion dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion;
    np:hasProvenance dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_provenance;
    np:hasPublicationInfo dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion a np:Assertion .
  
  dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_provenance a np:Provenance .
  
  dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion {
  miriam-gene:3565 a ncit:C16612 .
  
  lld:C2732618 a ncit:C7057 .
  
  dgn-gda:DGNb57156d89e6ba4d80a9e59c66408d1d7 sio:SIO_000628 miriam-gene:3565, lld:C2732618;
    a sio:SIO_001121 .
}

dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_provenance {
  dgn-np:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_assertion dcterms:description
      "[Altogether ten Single Nucleotide Polymorphisms (SNPs) of IL17A (rs2275913), IL17F (rs763780), IL4 (rs2243250), IL12A (rs583911), IL12B (rs3212227 and (rs17860508), IL23R (rs7517847), CXCL1 (rs4074), CXCL5 (rs425535) and CXCR2 (rs2230054) genes were genotyped by PCR with sequence specific primers (SSP) in 98 patients with PJI and two control groups 1) an aseptic TJA control (253 patients with TJA that did not develop PJI at least 6 yrs.]. 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:22660232;
    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:NP863301.RAupnG-FkC-SKsyOytHD0RHfxV4HBbc7x7bnSm4eRlcaE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:47+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" .
}