@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s> .
@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:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_head {
  this: np:hasAssertion dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_assertion;
    np:hasProvenance dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_provenance;
    np:hasPublicationInfo dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_assertion a np:Assertion .
  
  dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_provenance a np:Provenance .
  
  dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_assertion {
  miriam-gene:6690 a ncit:C16612 .
  
  lld:C0149521 a ncit:C7057 .
  
  dgn-gda:DGN44e87be9ea622ba0f1e5fef4dc21a6a3 sio:SIO_000628 miriam-gene:6690, lld:C0149521;
    a sio:SIO_001122 .
}

dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_provenance {
  dgn-np:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_assertion dcterms:description
      "[Although 45% of the study's ICP patients carried predisposing genetic risk factors (for example, mutations in CFTR or SPINK1), the authors found no evidence that the risk conveyed by CFTR mutations depends on co-inherited SPINK1 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:15987793;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP51130.RA9OcOJ972i4Q_tHj9iDx2Rhim58wEyf6Ugiiu83aSu7s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:23+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" .
}