@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY> .
@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:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_head {
  this: np:hasAssertion dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_assertion;
    np:hasProvenance dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_provenance;
    np:hasPublicationInfo dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_assertion a np:Assertion .
  
  dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_provenance a np:Provenance .
  
  dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_assertion {
  miriam-gene:3570 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN89f947f4b6e5c48bd85894ba88eaa263 sio:SIO_000628 miriam-gene:3570, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_provenance {
  dgn-np:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_assertion dcterms:description
      "[Although a common, non-synonymous variant in the IL-6 receptor gene (IL6R Asp358Ala; rs2228145 A>C) is associated with the risk of several common diseases, with the 358Ala allele conferring protection from coronary heart disease (CHD), rheumatoid arthritis (RA), atrial fibrillation (AF), abdominal aortic aneurysm (AAA), and increased susceptibility to asthma, the variant's effect on IL-6 signaling is not known.]. 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:23593036;
    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:NP465323.RADnB1k3pAHK4jrXPbTkVIMQrXVi88Ukern_bWlDaoiWY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:39+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" .
}