@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc> .
@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:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_head {
  this: np:hasAssertion dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion;
    np:hasProvenance dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_provenance;
    np:hasPublicationInfo dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion a np:Assertion .
  
  dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_provenance a np:Provenance .
  
  dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion {
  miriam-gene:6387 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN9936de86424ad695144130ab7dbc8595 sio:SIO_000628 miriam-gene:6387, lld:C0004096;
    a sio:SIO_001121 .
}

dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_provenance {
  dgn-np:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_assertion dcterms:description
      "[Among CXC chemokines, single nucleotide polymorphisms (SNPs) in the CXCL8 and CXCL12 genes stand out, as they have alleles associated with many diseases such as asthma and human immunodeficiency virus (HIV), respectively.]. 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:17848170;
    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:NP669516.RAaxOhIcYFDNXwq1v7nWZE1-i4LI7CuESvLXQWHwg_1fc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:44+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" .
}