@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ> .
@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:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_head {
  this: np:hasAssertion dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_assertion;
    np:hasProvenance dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_provenance;
    np:hasPublicationInfo dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_assertion a np:Assertion .
  
  dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_provenance a np:Provenance .
  
  dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_assertion {
  miriam-gene:10544 a ncit:C16612 .
  
  lld:C1719672 a ncit:C7057 .
  
  dgn-gda:DGNf557054269ba6a0ec196c6e9d5172256 sio:SIO_000628 miriam-gene:10544, lld:C1719672;
    a sio:SIO_001121 .
}

dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_provenance {
  dgn-np:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_assertion dcterms:description
      "[These results suggest that the EPCR- and PAR-1-dependent protective effects of APC in severe sepsis may partially be mediated through the inhibition of HMGB1 signaling and that the chimeric thrombin mutant has potential therapeutic utility for severe sepsis.]. 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:21849480;
    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:NP692191.RA_QMBSjDBw4koDDoXApdCKU4-qz83vowYReqR_0JaWQQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}