@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_head {
  this: np:hasAssertion dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion;
    np:hasProvenance dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_provenance;
    np:hasPublicationInfo dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion a np:Assertion .
  
  dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_provenance a np:Provenance .
  
  dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0009324 a ncit:C7057 .
  
  dgn-gda:DGN162d133423ed223047b933328de3e9ea sio:SIO_000628 miriam-gene:7099, lld:C0009324;
    a sio:SIO_001122 .
}

dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_provenance {
  dgn-np:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_assertion dcterms:description
      "[We observed that the R702W and 1007fs Nod2 alleles and the A299G Tlr4 alleles were significantly more prevalent in patients with CD as compared to healthy controls or patients with ulcerative colitis.]. 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:16010583;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP94092.RAtJn9w4EW7z9WhLJq__rc4DWjmUfcmRcZ7IAkIgWp_tk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:30+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}