@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c> .
@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 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:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_head {
  this: np:hasAssertion dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion;
    np:hasProvenance dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance;
    np:hasPublicationInfo dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion a np:Assertion .
  
  dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance a np:Provenance .
  
  dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN4aa8cf469b6aa601889e26a3352bbece sio:SIO_000628 miriam-gene:64127, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_provenance {
  dgn-np:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_assertion dct:description
      "[The CARD15 R702W variant might be a predisposing factor to sporadic CRC in Portugal, particularly in patients under 60-years old and in female patients. This susceptibility appears to be linked with germline CARD15 mutations. Nevertheless, we have found no evidence that CARD15 mutations predict the pathologic characteristics of CRC.]. 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:20676658;
    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:NP47618.RAhuLh7kOZcrieIyBJF9_5_4Jxr960KaG10WW2L1pXF-c130_publicationInfo {
  this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}