@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s> .
@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:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_head {
  this: np:hasAssertion dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_assertion;
    np:hasProvenance dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_provenance;
    np:hasPublicationInfo dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_assertion a np:Assertion .
  
  dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_provenance a np:Provenance .
  
  dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_assertion {
  miriam-gene:990 a ncit:C16612 .
  
  lld:C0024117 a ncit:C7057 .
  
  dgn-gda:DGN6805ff19a58b7b47052d8b46e177a9ac sio:SIO_000628 miriam-gene:990, lld:C0024117;
    a sio:SIO_001122 .
}

dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_provenance {
  dgn-np:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_assertion dct:description
      "[We tested our hypothesis that the individual susceptibility to rapid decline in lung function despite smoking cessation in patients with advanced stages of COPD is attributed to the genetic variants in the CDC6 gene.]. 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:19233139;
    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:NP78425.RA-wb9_swSSGgTt32QxcOG88JqDscLyC6KXdy7fUlea_s130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+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" .
}