@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE> .
@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:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_head {
  this: np:hasAssertion dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_assertion;
    np:hasProvenance dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_provenance;
    np:hasPublicationInfo dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_assertion a np:Assertion .
  
  dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_provenance a np:Provenance .
  
  dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_assertion {
  miriam-gene:64127 a ncit:C16612 .
  
  lld:C1275126 a ncit:C7057 .
  
  dgn-gda:DGNcb558e3f20f757c2c11c91a95a3857a1 sio:SIO_000628 miriam-gene:64127, lld:C1275126;
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dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_provenance {
  dgn-np:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_assertion dcterms:description
      "[Given the pathological similarities between Behçet's disease (BD), Familial Mediterranean fever (FMF), TNF receptor-associated periodic syndrome (TRAPS) and Crohn's disease (CD) we evaluated the frequency of mutations and polymorphisms in MEFV, TNFRSF1A and CARD15 in Israeli BD patients of either Jewish or Arab descent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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    prov:wasDerivedFrom dgn-void:befree-2016;
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  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:NP877994.RA9lp2JiC8TjIaDJR2cBN_PFe5mevGh2fseWPREBzn1zE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:22+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}