@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc> .
@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:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_head {
  this: np:hasAssertion dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion;
    np:hasProvenance dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_provenance;
    np:hasPublicationInfo dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion a np:Assertion .
  
  dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_provenance a np:Provenance .
  
  dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN2ffd987e96daa6b38653989354bf6097 sio:SIO_000628 miriam-gene:7099, lld:C0010674;
    a sio:SIO_001122 .
}

dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_provenance {
  dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion dcterms:description
      "[Potential reasons for absence of modifier effect include the basolateral location of TLR4 receptors on respiratory epithelium, or because inflammatory response to PA in the CF airway is so overwhelming that even a blunted response (as suggested for the 299G allele) results in increased inflammation and lung damage.]. 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:16830219;
    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:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}