@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE> .
@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:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_head {
   this: np:hasAssertion dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_assertion ;
    np:hasProvenance dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_provenance ;
    np:hasPublicationInfo dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_assertion a np:Assertion .
  dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_provenance a np:Provenance .
  dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_assertion {
   miriam-gene:875 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
  dgn-gda:DGN113f390655d00b87f591bf38fe8cb464 sio:SIO_000628 miriam-gene:875 , lld:C1956346 ;
    a sio:SIO_001121 .
}
dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_provenance {
   dgn-np:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_assertion dcterms:description "[The combined group samples identified 6 up regulated differential expression (DE) genes (GHRL, LTA, CBS, HP, ITGA2B, and OLR1) and 12 down regulated DE genes (IL18R1, ITGA2B, IL18RAP, HP, OLR1, SOD2 ITGB3, IL1B, MMP9, PLA2G7, UTS2, and CBS) to be involved in CAD at the fold change of 1.3 with fault discovery rate (FDR) of 1%.]. 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:22738689 ;
    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:NP993494.RAFN61xnK8kwlgUVaU71wxMJxIasy9v3nuSyTyPV0BFGE130_publicationInfo {
   this: dcterms:created "2016-05-13T12:49:15+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: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" .
}