@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ> .
@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:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_head {
  this: np:hasAssertion dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_assertion;
    np:hasProvenance dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_assertion a np:Assertion .
  
  dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_provenance a np:Provenance .
  
  dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_assertion {
  miriam-gene:6556 a ncit:C16612 .
  
  lld:C0024115 a ncit:C7057 .
  
  dgn-gda:DGNd67ffca620886ada41a0e4e05503d77e sio:SIO_000628 miriam-gene:6556, lld:C0024115;
    a sio:SIO_001121 .
}

dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_provenance {
  dgn-np:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_assertion dcterms:description
      "[Subjects who were heterozygous for two NRAMP1 polymorphisms in INT4 and D543N were particularly overrepresented among those with NTM lung disease, compared with those with the most common NRAMP1 genotype (OR, 10.88, 95% CI, 1.18 to 100.45; p = 0.035).]. 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:16002921;
    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:NP206302.RA3CnaCCfPyoIR0ZVIdZCMuohWsUBgIJ510RNo1baSQUQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+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" .
}