@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc> .
@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:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_head {
  this: np:hasAssertion dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_assertion;
    np:hasProvenance dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_provenance;
    np:hasPublicationInfo dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_assertion a np:Assertion .
  
  dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_provenance a np:Provenance .
  
  dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_assertion {
  miriam-gene:2524 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN467040ed343d4a0993a8c60e85bfc016 sio:SIO_000628 miriam-gene:2524, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_provenance {
  dgn-np:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_assertion dcterms:description
      "[Polymorphisms in the genes encoding ABO blood type, secretor or Lewis genotypes were not shown to associate with severity of CF lung disease, or age of onset of P. aeruginosa infection, nor was there any association with other clinical phenotypes in a group of 808 patients homozygous for the DeltaF508 mutation.]. 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:19169360;
    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:NP173331.RAAQXrtYQcfDvJU_eurmc2lC-WfL6fWW1fmTuUBGkWYcc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:33+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" .
}