@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0> .
@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:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_head {
  this: np:hasAssertion dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_assertion;
    np:hasProvenance dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_provenance;
    np:hasPublicationInfo dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_assertion a np:Assertion .
  
  dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_provenance a np:Provenance .
  
  dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_assertion {
  miriam-gene:6584 a ncit:C16612 .
  
  lld:C0021390 a ncit:C7057 .
  
  dgn-gda:DGNe7b2a4ce83fa3249d892ab30f620b3d5 sio:SIO_000628 miriam-gene:6584, lld:C0021390;
    a sio:SIO_001122 .
}

dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_provenance {
  dgn-np:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_assertion dcterms:description
      "[Our results indicate that although OCTN or CARD15 variation is associated with susceptibility to IBD in Western populations, these might be rare and may not be associated with susceptibility to IBD in Chinese patients.]. 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:18756601;
    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:NP81572.RAIPgYMgO5MnWjCocGQRk_UFMBZUAeOHXQCtSJvxZNQl0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:40+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" .
}