@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs> .
@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:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_head {
  this: np:hasAssertion dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_assertion ;
    np:hasProvenance dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_provenance ;
    np:hasPublicationInfo dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_provenance a np:Provenance .
  dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_assertion {
  miriam-gene:3557 a ncit:C16612 .
  lld:C0010346 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_provenance {
  dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_assertion dcterms:description "[The aim of this study was to determine the association of polymorphisms in the CARD15, TNFA, IL1B, and IL1RN genes with risk of development of CD and with the clinicopathological profile of CD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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}
dgn-np:NP322437.RAaqzsoN67k7KWVcUvAxO_6QEzpBnOtPOrNdEEaTBqWqs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:08+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}