@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg> .
@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:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_head {
  this: np:hasAssertion dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion;
    np:hasProvenance dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_provenance;
    np:hasPublicationInfo dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion a np:Assertion .
  
  dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_provenance a np:Provenance .
  
  dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion {
  miriam-gene:6285 a ncit:C16612 .
  
  lld:C0022116 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_provenance {
  dgn-np:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_assertion dcterms:description
      "[Hence, S100B, far from being a negative determinant of outcome, as suggested previously in the human TBI and ischemia literature, is of potential therapeutic value that could improve outcome in patients who sustain various forms of acute brain damage.]. 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:16928177;
    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:NP539193.RAhxlo-ZJP8LHJVptr26HFAMQPREPuFN28WHWw361pxSg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:25+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>;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}