@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8> .
@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:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_head {
  this: np:hasAssertion dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_assertion;
    np:hasProvenance dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_provenance;
    np:hasPublicationInfo dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_assertion a np:Assertion .
  
  dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_provenance a np:Provenance .
  
  dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_assertion {
  miriam-gene:3553 a ncit:C16612 .
  
  lld:C0004943 a ncit:C7057 .
  
  dgn-gda:DGN92d24beb8994f82bc08ec5980a0c53cf sio:SIO_000628 miriam-gene:3553, lld:C0004943;
    a sio:SIO_001121 .
}

dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_provenance {
  dgn-np:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_assertion dcterms:description
      "[In the current study of Behçet disease (BD), nonsynonymous variants (NSVs) identified by deep exonic resequencing of 10 genes found by GWAS (IL10, IL23R, CCR1, STAT4, KLRK1, KLRC1, KLRC2, KLRC3, KLRC4, and ERAP1) and 11 genes selected for their role in innate immunity (IL1B, IL1R1, IL1RN, NLRP3, MEFV, TNFRSF1A, PSTPIP1, CASP1, PYCARD, NOD2, and TLR4) were evaluated for BD association.]. 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:23633568;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1073907.RA1JUp1L8_W_x0u54BNomfLZLYsSfZ4czzpOiPHXzYxK8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:53+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}