@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA> .
@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:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_head {
  this: np:hasAssertion dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_assertion ;
    np:hasProvenance dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_provenance ;
    np:hasPublicationInfo dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_assertion a np:Assertion .
  dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_provenance a np:Provenance .
  dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_assertion {
  miriam-gene:6690 a ncit:C16612 .
  lld:C0856281 a ncit:C7057 .
  dgn-gda:DGN07d2b9ce5adcbf2fc9b3c4a6e80cf42a sio:SIO_000628 miriam-gene:6690 , lld:C0856281 ;
    a sio:SIO_001121 .
}
dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_provenance {
  dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_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 ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP163181.RAZuFHmo1kApNz7jv746WUxj_nLgfgZslNI-DTU34ljIA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:28+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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}