@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI> .
@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:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_head {
  this: np:hasAssertion dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_assertion;
    np:hasProvenance dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_provenance;
    np:hasPublicationInfo dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_assertion a np:Assertion .
  
  dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_provenance a np:Provenance .
  
  dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0009324 a ncit:C7057 .
  
  dgn-gda:DGN9823f121e67227c0f70090c51aed358c sio:SIO_000628 miriam-gene:3133, lld:C0009324;
    a sio:SIO_001121 .
}

dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_provenance {
  dgn-np:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_assertion dcterms:description
      "[We now have a much more detailed appreciation of the molecular genetic architecture of inflammatory bowel disease (IBD), and particularly the areas of overlap between Crohn's disease (CD) and ulcerative colitis (UC) (such as Th17 pathways) and the pathways which are disease-specific (such as NOD2 and autophagy for CD and the MHC and epithelial barrier genes for UC).]. 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:23075873;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP217315.RAk3elbzQmNknrASKWV9xyYGInmm9mDgcUD45yI_1VujI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:00+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" .
}