@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4> .
@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:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_head {
  this: np:hasAssertion dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_assertion;
    np:hasProvenance dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_provenance;
    np:hasPublicationInfo dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_assertion a np:Assertion .
  
  dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_provenance a np:Provenance .
  
  dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_assertion {
  miriam-gene:4210 a ncit:C16612 .
  
  lld:C0010346 a ncit:C7057 .
  
  dgn-gda:DGNc0a098ab143b61a0a3c31f5f058dbded sio:SIO_000628 miriam-gene:4210, lld:C0010346;
    a sio:SIO_001121 .
}

dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_provenance {
  dgn-np:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_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;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:21385537;
    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:NP240880.RAUOVDsjrVEr4fbngLtS2RdvGtU1C4bN58ritWUIbt_V4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:15+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" .
}