@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw> .
@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:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_head {
  this: np:hasAssertion dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion;
    np:hasProvenance dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_provenance;
    np:hasPublicationInfo dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion a np:Assertion .
  
  dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_provenance a np:Provenance .
  
  dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0151317 a ncit:C7057 .
  
  dgn-gda:DGN647fcecd8046dacca3b76dab607378c2 sio:SIO_000628 miriam-gene:1080, lld:C0151317;
    a sio:SIO_001121 .
}

dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_provenance {
  dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion dcterms:description
      "[The CFTR mutations in cystic fibrosis (CF) lead to ion transport anomalities which predispose to chronic infection and inflammation of CF airways as the major determinants for morbidity and mortality in CF.]. 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:16463024;
    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:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+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" .
}