@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU> .
@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:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_head {
  this: np:hasAssertion dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion;
    np:hasProvenance dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_provenance;
    np:hasPublicationInfo dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion a np:Assertion .
  
  dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_provenance a np:Provenance .
  
  dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion {
  miriam-gene:10392 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN9c501bdf04e39821a4550a5031c0c7fb sio:SIO_000628 miriam-gene:10392, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_provenance {
  dgn-np:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_assertion dct:description
      "[Since the CARD15 gene product and other CARD proteins function in innate immunity, we investigated the impact of germline variation at the CARD4, CARD8 and CARD15 loci on the risk for sporadic CRC, using a large patient sample from Northern Germany.]. 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:19843337;
    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:NP78763.RA-HC-mhKGNfkX4d7PsGQUnJM6MvXbBrHTCLa49TOKiwU130_publicationInfo {
  this: dct:created "2014-10-02T12:32:38+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" .
}