@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900> .
@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:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_head {
  this: np:hasAssertion dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_assertion;
    np:hasProvenance dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_provenance;
    np:hasPublicationInfo dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_assertion a np:Assertion .
  
  dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_provenance a np:Provenance .
  
  dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_assertion {
  miriam-gene:3576 a ncit:C16612 .
  
  lld:C1800706 a ncit:C7057 .
  
  dgn-gda:DGN4d2b036d9bedddbf8ab26fa38bd71544 sio:SIO_000628 miriam-gene:3576, lld:C1800706;
    a sio:SIO_001121 .
}

dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_provenance {
  dgn-np:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_assertion dcterms:description
      "[To search for single-nucleotide polymorphisms in the interleukin-8 (IL-8) and IL-8 receptor CXCR-1 and CXCR-2 genes, and to compare their distribution among patients with systemic sclerosis (SSc) with fibrosing alveolitis (FASSc) or without fibrosing alveolitis (NFASSc), or patients with cryptogenic fibrosing alveolitis (CFA), and normal healthy subjects.]. 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:10902769;
    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:NP154449.RA1yuPzzobpd6RGycqHyKzK7y9G2C0grNidcH_wpXX900130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}