@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I> .
@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:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_head {
   this: np:hasAssertion dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_assertion ;
    np:hasProvenance dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_provenance ;
    np:hasPublicationInfo dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_assertion a np:Assertion .
  dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_provenance a np:Provenance .
  dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_assertion {
   miriam-gene:102724560 a ncit:C16612 .
  lld:C1956346 a ncit:C7057 .
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}
dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_provenance {
   dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_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-20150227 ;
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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 ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP1018469.RA8AbqoSnOng_Ztg_q5k9bf43o9hn5oyAPF4h0UmFHZ1I130_publicationInfo {
   this: dcterms:created "2015-08-25T14:48:12+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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    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> ;
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}