@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_head {
  this: np:hasAssertion dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_assertion;
    np:hasProvenance dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_provenance;
    np:hasPublicationInfo dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_assertion a np:Assertion .
  
  dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_provenance a np:Provenance .
  
  dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0024115 a ncit:C7057 .
  
  dgn-gda:DGN9b55617a873517f55e2e6d416d57f5b9 sio:SIO_000628 miriam-gene:1080, lld:C0024115;
    a sio:SIO_001121 .
}

dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_provenance {
  dgn-np:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_assertion dcterms:description
      "[This study suggests that the phenotype of adult cystic fibrosis patients, including the severity of the lung disease, is related to the severity of the cystic fibrosis transmembrane conductance regulator mutations.]. 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:8947061;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1363654.RA9_eVwjAgWMlYVJ9Jfm1v4vv43vbhnQtv9ti1rYNE3fE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:04+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}