@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_head {
  this: np:hasAssertion dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_assertion ;
    np:hasProvenance dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_provenance ;
    np:hasPublicationInfo dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_assertion a np:Assertion .
  dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_provenance a np:Provenance .
  dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_assertion {
  miriam-gene:7473 a ncit:C16612 .
  lld:C0024115 a ncit:C7057 .
  dgn-gda:DGN7790af24c90cf20fe2cb003d6a0a49de sio:SIO_000628 miriam-gene:7473 , lld:C0024115 ;
    a sio:SIO_001122 .
}
dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_provenance {
  dgn-np:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_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-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP777322.RAdeZzeB35kvSzyZRG3QH0jewoInLUz0aFPEcw3nSNcok130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:30+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}