@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U> .
@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:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_head {
  this: np:hasAssertion dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_assertion;
    np:hasProvenance dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_provenance;
    np:hasPublicationInfo dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_assertion a np:Assertion .
  
  dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_provenance a np:Provenance .
  
  dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_assertion {
  miriam-gene:5595 a ncit:C16612 .
  
  lld:C0151744 a ncit:C7057 .
  
  dgn-gda:DGN1a7778ad32cffe530d949aa975c8274b sio:SIO_000628 miriam-gene:5595, lld:C0151744;
    a sio:SIO_001121 .
}

dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_provenance {
  dgn-np:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_assertion dcterms:description
      "[Hence, while CB2, PLC and PKC, ERK1/2, and eNOS are more strongly expressed in patients without ischemic heart disease, high CB1 and PKA expression is associated with low survival intracellular pathway activation and high iNOS activation in ischemic heart disease patients.]. 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:22926037;
    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:NP300386.RAi1lq79EOt_OR8a3g_9ifchVwIfLpg8qOPfWGc-BZ37U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}