@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE> .
@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:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_head {
  this: np:hasAssertion dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion ;
    np:hasProvenance dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_provenance ;
    np:hasPublicationInfo dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion a np:Assertion .
  dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_provenance a np:Provenance .
  dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion {
  miriam-gene:6690 a ncit:C16612 .
  lld:C0271642 a ncit:C7057 .
  dgn-gda:DGN653ca3c39743e9b1fcea537f7b8c3cc3 sio:SIO_000628 miriam-gene:6690 , lld:C0271642 ;
    a sio:SIO_001121 .
}
dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_provenance {
  dgn-np:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_assertion dcterms:description "[Since SPINK1 mutations in Europeans and North Americans are associated with idiopathic chronic pancreatitis that is phenotypically different from FCPD, we further conclude that mutated SPINK1 markedly increases the risk of developing a variety of pancreatic diseases possibly through a chronic elevation of active trypsin within the pancreas.]. 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:12120202 ;
    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:NP724495.RA8WzTzdzcHzAfpWJYtlxANL2lIu7vVm8VjNhkdBChheE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:19+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" .
}