@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4> .
@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:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_head {
  this: np:hasAssertion dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_assertion;
    np:hasProvenance dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_provenance;
    np:hasPublicationInfo dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_assertion a np:Assertion .
  
  dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_provenance a np:Provenance .
  
  dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0024117 a ncit:C7057 .
  
  dgn-gda:DGN76430cd56e27e4747b9f93f64dcf3b8d sio:SIO_000628 miriam-gene:5265, lld:C0024117;
    a sio:SIO_001121 .
}

dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_provenance {
  dgn-np:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_assertion dcterms:description
      "[The aim of our study was to determine the genetic risk conferred by SNPs in the SERPINA1 and ADRB2 for development of Chronic Obstructive Pulmonary Disease (COPD) and Disseminated Bronchiectasis (DB), while at the same time validating the NanoChip technology.]. 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:19747908;
    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:NP338372.RA2yzsXJmGMcEP43lVqnr0EYjVjBjj13Yuro4ZFALlNf4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:19+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" .
}