@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_head {
  this: np:hasAssertion dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion;
    np:hasProvenance dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_provenance;
    np:hasPublicationInfo dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion a np:Assertion .
  
  dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_provenance a np:Provenance .
  
  dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion {
  miriam-gene:6690 a ncit:C16612 .
  
  lld:C0149521 a ncit:C7057 .
  
  dgn-gda:DGN6b63f0ca374615fb2d5a4185eccc5414 sio:SIO_000628 miriam-gene:6690, lld:C0149521;
    a sio:SIO_001121 .
}

dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_provenance {
  dgn-np:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_assertion dcterms:description
      "[Mutations in three genes, the cationic trypsinogen (PRSS1) gene, the cystic fibrosis transmembrane conductance regulator (CFTR) gene and the pancreatic secretory trypsin inhibitor (SPINK1) gene, have been identified as risk factors for CP.]. 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:22109105;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP710391.RAGXe2YPdMyhlvl-_FX-xGuReRRHrbjE_F5XAVl_LvhOc130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:48+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}