@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ> .
@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:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_head {
  this: np:hasAssertion dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion;
    np:hasProvenance dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_provenance;
    np:hasPublicationInfo dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion a np:Assertion .
  
  dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_provenance a np:Provenance .
  
  dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0856281 a ncit:C7057 .
  
  dgn-gda:DGNcb0df45e5956ad136b1a9123207f9a58 sio:SIO_000628 miriam-gene:1080, lld:C0856281;
    a sio:SIO_001121 .
}

dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_provenance {
  dgn-np:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_assertion dcterms:description
      "[In a population-based, well-defined group of patients first regarded as having pancreatitis of unknown origin (PUO), we identified, described, and compared the clinical and genetic aspects of patients with hereditary pancreatitis (HP) and with cystic fibrosis transmembrane conductance regulator gene (CFTR) and serine protease inhibitor Kazal type 1 gene (SPINK1) mutations with patients who retained the diagnosis of true idiopathic pancreatitis (tIP) after genetic testing for HP, SPINK1, and CFTR 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:20502448;
    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:NP354428.RAAsljFGsPHF0lkBkFrzkKrEZn-Pip4FRrIrpsr5LsfiQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:28+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" .
}