@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM> .
@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:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_head {
  this: np:hasAssertion dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_assertion;
    np:hasProvenance dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_provenance;
    np:hasPublicationInfo dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_assertion a np:Assertion .
  
  dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_provenance a np:Provenance .
  
  dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_assertion {
  miriam-gene:6347 a ncit:C16612 .
  
  lld:C0023288 a ncit:C7057 .
  
  dgn-gda:DGNbe68b9cf60e963f4795b3fdd4cf4cf38 sio:SIO_000628 miriam-gene:6347, lld:C0023288;
    a sio:SIO_001121 .
}

dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_provenance {
  dgn-np:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_assertion dcterms:description
      "[The GG recessive genotype at CCL2 -2518bp was more common in patients with ML (N=67) than in neighborhood control (NC; N=60) subjects (OR 1.78; 95% CI 1.01-3.14; P=0.045), than in NC combined with leishmanin skin-test positive (N=60) controls (OR 4.40; 95% CI 1.42-13.65; P=0.010), and than in controls combined with CL (N=60) patients (OR 2.78; 95% CI 1.13-6.85; P=0.045).]. 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:20430117;
    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:NP429953.RAeUBe25b3Ap7pOfR3DdyDOo7uJf0p7gFcZOmdw4NtzZM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:15+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" .
}