@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8> .
@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:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_head {
  this: np:hasAssertion dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_assertion;
    np:hasProvenance dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_provenance;
    np:hasPublicationInfo dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_assertion a np:Assertion .
  
  dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_provenance a np:Provenance .
  
  dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_assertion {
  miriam-gene:3579 a ncit:C16612 .
  
  lld:C0036421 a ncit:C7057 .
  
  dgn-gda:DGNea56c1578f3bd44fd0c64faf766859d8 sio:SIO_000628 miriam-gene:3579, lld:C0036421;
    a sio:SIO_001121 .
}

dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_provenance {
  dgn-np:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_assertion dcterms:description
      "[In the present study, we investigated the influence of variation in the CXCL8 and CXCR2 genes on susceptibility to SSc and combined the variant alleles of these genes to analyze their effects on SSc.]. 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:22763041;
    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:NP529009.RASZZjRZ-Z1jqnRZcRiKPwM1HTfOvs-opQRT5Nv3VSsp8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:19+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" .
}