@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8> .
@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:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_head {
  this: np:hasAssertion dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_assertion;
    np:hasProvenance dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_provenance;
    np:hasPublicationInfo dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_assertion a np:Assertion .
  
  dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_provenance a np:Provenance .
  
  dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN4288e03aa6d34e88d16d67268ef489e4 sio:SIO_000628 miriam-gene:64127, lld:C1527249;
    a sio:SIO_001122 .
}

dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_provenance {
  dgn-np:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_assertion dcterms:description
      "[described an association between the 3020insC NOD2 single nucleotide polymorphism and the risk of colorectal cancer(CRC) in 2004, reports published in the past several years have controversial results regarding the relationship between the development of CRC and NOD2 gene polymorphisms.]. 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:19787357;
    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:NP47616.RAy59xpcN8V4ugIKMjVZipCp3l9w9X0X37hh-THJwFoS8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}