@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg> .
@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:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_head {
  this: np:hasAssertion dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_assertion;
    np:hasProvenance dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_provenance;
    np:hasPublicationInfo dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_assertion a np:Assertion .
  
  dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_provenance a np:Provenance .
  
  dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_assertion {
  miriam-gene:5644 a ncit:C16612 .
  
  lld:C2931038 a ncit:C7057 .
  
  dgn-gda:DGN648ed8938dedbb42a308eec4b21b0fd4 sio:SIO_000628 miriam-gene:5644, lld:C2931038;
    a sio:SIO_001121 .
}

dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_provenance {
  dgn-np:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_assertion dcterms:description
      "[Of 60 families identified by the UK and Ireland consortium of EUROPAC (European Registry for Hereditary Pancreatitis and Familial Pancreatic Cancer), 51 were screened for R122H, N29I, and A16V mutations using standard techniques, and by sequencing of all five exons of cationic trypsinogen.]. 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:11156648;
    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:NP440919.RARTcvoKu-o5k696QGzvWRpNCvhqsZCwJNv8ZKF2d88Rg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:21+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" .
}