@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978> .
@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:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_head {
  this: np:hasAssertion dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_assertion;
    np:hasProvenance dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_provenance;
    np:hasPublicationInfo dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_assertion a np:Assertion .
  
  dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_provenance a np:Provenance .
  
  dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_publicationInfo a
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}

dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_assertion {
  miriam-gene:3557 a ncit:C16612 .
  
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dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_provenance {
  dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_assertion dcterms:description
      "[Using RT-PCR to determine the expression pattern of the IL1RN isoforms, we found different expression patterns between normal controls and patients with SLE, with an addition of IL1RN isoform4 or the low expression of IL1RN isoform1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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 .
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dgn-np:NP160246.RAfUF07SaelYYFWa86wX_swhAp6XqvnobIU0QvgzpY978130_publicationInfo {
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    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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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