@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs> .
@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:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_head {
  this: np:hasAssertion dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_assertion;
    np:hasProvenance dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_provenance;
    np:hasPublicationInfo dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_assertion a np:Assertion .
  
  dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_provenance a np:Provenance .
  
  dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_assertion {
  miriam-gene:84639 a ncit:C16612 .
  
  lld:C0038013 a ncit:C7057 .
  
  dgn-gda:DGNd020556b71eed4fa1db1a369afcc02d5 sio:SIO_000628 miriam-gene:84639, lld:C0038013;
    a sio:SIO_001122 .
}

dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_provenance {
  dgn-np:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_assertion dcterms:description
      "[Nine polymorphisms in the IL1 gene cluster members IL1A (rs2856836, rs17561 and rs1894399), IL1B (rs16944), IL1F10 (rs3811058) and IL1RN (rs419598, the IL1RA VNTR, rs315952 and rs315951) were genotyped in 2675 AS cases and 2592 healthy controls recruited in 12 different centres in 10 countries.]. 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:18063673;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP67428.RAzygFcxvrkP1wfBq0bssb9_8Lcxei20SmlB_HYU0abCs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}