@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc> .
@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:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_head {
  this: np:hasAssertion dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion;
    np:hasProvenance dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_provenance;
    np:hasPublicationInfo dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion a np:Assertion .
  
  dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_provenance a np:Provenance .
  
  dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion {
  miriam-gene:3991 a ncit:C16612 .
  
  lld:C0024117 a ncit:C7057 .
  
  dgn-gda:DGNd743317eb4769173c6fdb177b5f37313 sio:SIO_000628 miriam-gene:3991, lld:C0024117;
    a sio:SIO_001121 .
}

dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_provenance {
  dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion dcterms:description
      "[Polymorphisms that were associated with lung function level or rate of decline in the Lung Health Study (LHS) cohort were analyzed for association with COPD affection status in four other COPD case-control populations.]. 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:22200767;
    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:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:57+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" .
}