@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc> .
@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:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_head {
  this: np:hasAssertion dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_assertion;
    np:hasProvenance dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_provenance;
    np:hasPublicationInfo dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_assertion a np:Assertion .
  
  dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_provenance a np:Provenance .
  
  dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_assertion {
  miriam-gene:671 a ncit:C16612 .
  
  lld:C0243026 a ncit:C7057 .
  
  dgn-gda:DGN25b087dd7637ac2b1985223a6c8e7e58 sio:SIO_000628 miriam-gene:671, lld:C0243026;
    a sio:SIO_001122 .
}

dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_provenance {
  dgn-np:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_assertion dcterms:description
      "[ Our findings suggest that common polymorphisms in the gene for LBP in combination with male gender are associated with an increased risk for the development of sepsis and, furthermore, may be linked to an unfavorable outcome. These data support the important immunomodulatory role of LBP in Gram-negative sepsis and suggest that genetic testing may be helpful for the identification of patients with an unfavorable response to Gram-negative infection.]. 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:11373419;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP62742.RArwmf0Q7V2UZ4MlOlZl2gIG_ah9ciREgreDE6hAZ0KSc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}