@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus> .
@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 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:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_head {
  this: np:hasAssertion dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion ;
    np:hasProvenance dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance ;
    np:hasPublicationInfo dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion a np:Assertion .
  dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance a np:Provenance .
  dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion {
  miriam-gene:929 a ncit:C16612 .
  lld:C0477474 a ncit:C7057 .
  dgn-gda:DGN21e84266892dd577335746bd32008e48 sio:SIO_000628 miriam-gene:929 , lld:C0477474 ;
    a sio:SIO_001122 .
}
dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_provenance {
  dgn-np:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_assertion dct:description "[ Our results contradict previous reports that have found a protective effect of the T allele of SNP rs2569190 (C-159T) against atopic disorders. Nevertheless, these results confirm the importance of polymorphisms in CD14 in the development of atopy, and future studies of this gene region will need to account for linkage disequilibrium and environmental exposures unique to the study population.]. 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:15867866 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP47186.RApmY-N3pgJ4y1YCnKXHkBRhTqXxpblz_953z53FK-Dus130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}