@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A> .
@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:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_head {
  this: np:hasAssertion dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_assertion;
    np:hasProvenance dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_provenance;
    np:hasPublicationInfo dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_assertion a np:Assertion .
  
  dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_provenance a np:Provenance .
  
  dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  
  lld:C0009404 a ncit:C7057 .
  
  dgn-gda:DGNff864785e9d932c16ecbc5dc9ed5988c sio:SIO_000628 miriam-gene:64127, lld:C0009404;
    a sio:SIO_001122 .
}

dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_provenance {
  dgn-np:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_assertion dcterms:description
      "[Data show that the P286S, R702W, G908R, and 1007fs mutations of Nod2 were more frequent among colorectal cancer patients than controls and that the presence of the 1007fs variant might also be associated with young patient age.]. 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:18758419;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP106301.RATKQdo2fnfU6AJ3V9MTQ9iXXeu71_8pj-nGClkVkUk-A130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:54+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" .
}