@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM> .
@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:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_head {
  this: np:hasAssertion dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_assertion;
    np:hasProvenance dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_provenance;
    np:hasPublicationInfo dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_assertion a np:Assertion .
  
  dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_provenance a np:Provenance .
  
  dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0149521 a ncit:C7057 .
  
  dgn-gda:DGN23f976347879aaea4605208684003ab9 sio:SIO_000628 miriam-gene:1080, lld:C0149521;
    a sio:SIO_001122 .
}

dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_provenance {
  dgn-np:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_assertion dcterms:description
      "[DNA analyses of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in Japanese patients with idiopathic chronic pancreatitis (ICP) were performed to determine the relationship between the CFTR mutation and ICP.]. 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:19383231;
    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:NP62621.RAcFiyhxRdzfcBt9GueiwZ8oVVeOxTME-eXtaun-k-rOM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}