@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs> .
@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/v3.0.0/void/> .

dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_head {
  this: np:hasAssertion dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_assertion;
    np:hasProvenance dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_provenance;
    np:hasPublicationInfo dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_assertion a np:Assertion .
  
  dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_provenance a np:Provenance .
  
  dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_assertion {
  miriam-gene:25801 a ncit:C16612 .
  
  lld:C0039483 a ncit:C7057 .
  
  dgn-gda:DGNe2e9469e2c48c0f0b0af1039ebeefed9 sio:SIO_000628 miriam-gene:25801, lld:C0039483;
    a sio:SIO_001121 .
}

dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_provenance {
  dgn-np:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_assertion dcterms:description
      "[Similarly, when patients were stratified according to the specific clinical features of GCA such as polymyalgia rheumatica, visual ischaemic manifestations or irreversible occlusive disease, no statistical significant difference was detected either between the case subgroups and the control set or between GCA patients with and without the specific features of the disease.]. 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:23306142;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP878293.RAtbLitvTsRd_zE-wU2XCFfQ2yNclEAJ8GoWjSNFyg7Rs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:35+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}