@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E> .
@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:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_head {
  this: np:hasAssertion dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_assertion;
    np:hasProvenance dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_provenance;
    np:hasPublicationInfo dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_assertion a np:Assertion .
  
  dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_provenance a np:Provenance .
  
  dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_assertion {
  miriam-gene:3579 a ncit:C16612 .
  
  lld:C0024117 a ncit:C7057 .
  
  dgn-gda:DGNc2b566e025d3665112be32b986544b15 sio:SIO_000628 miriam-gene:3579, lld:C0024117;
    a sio:SIO_001121 .
}

dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_provenance {
  dgn-np:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_assertion dcterms:description
      "[With the development of several pharmacological, immunological and genetic tools to study CXCR2 function, an important role for this CXC chemokine receptor subtype has been identified in chronic obstructive pulmonary disease (COPD), asthma and fibrotic pulmonary disorders.]. 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:19026683;
    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:NP268471.RAActrwK2yYSe-tTZ3HG5gOjhJIybA-5w2gozOvYvag_E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:30+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" .
}