@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY> .
@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:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_head {
  this: np:hasAssertion dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_assertion;
    np:hasProvenance dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_provenance;
    np:hasPublicationInfo dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_assertion a np:Assertion .
  
  dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_provenance a np:Provenance .
  
  dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0149521 a ncit:C7057 .
  
  dgn-gda:DGN3302607505218ef233eaad7950fa23b1 sio:SIO_000628 miriam-gene:1080, lld:C0149521;
    a sio:SIO_001122 .
}

dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_provenance {
  dgn-np:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_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:NP62618.RAFGiIiaOHFIznah427K6ksjGcvsPHSpalFGJD8e_KBBY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}