@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo> .
@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:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_head {
  this: np:hasAssertion dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_assertion;
    np:hasProvenance dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_provenance;
    np:hasPublicationInfo dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_assertion a np:Assertion .
  
  dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_provenance a np:Provenance .
  
  dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_assertion {
  miriam-gene:7099 a ncit:C16612 .
  
  lld:C0699826 a ncit:C7057 .
  
  dgn-gda:DGNfe82d30e9cf74ec79181244df67474ef sio:SIO_000628 miriam-gene:7099, lld:C0699826;
    a sio:SIO_001121 .
}

dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_provenance {
  dgn-np:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_assertion dcterms:description
      "[The results showed that the expression of TLR4 and MAPK families are increased in the patients with acute coronary syndrome (ACS), compared with it in the patients with stable angina and controls.]. 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:18373609;
    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:NP534791.RAASPiIW2fPadw-kfDY9CC6667nCHhtI8msg8YSxebMEo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:23+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" .
}