@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M> .
@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:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_head {
  this: np:hasAssertion dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion;
    np:hasProvenance dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_provenance;
    np:hasPublicationInfo dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion a np:Assertion .
  
  dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_provenance a np:Provenance .
  
  dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion {
  miriam-gene:1672 a ncit:C16612 .
  
  lld:C1719672 a ncit:C7057 .
  
  dgn-gda:DGN803c71629d063f4ff29d697ef7e93254 sio:SIO_000628 miriam-gene:1672, lld:C1719672;
    a sio:SIO_001121 .
}

dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_provenance {
  dgn-np:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_assertion dcterms:description
      "[The present case-control study was designed to investigate whether DEFB1 genomic variations are associated with the susceptibility to and the outcome of severe sepsis in 211 patients with severe sepsis and 157 ethnic-matched healthy 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:17508030;
    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:NP535408.RAJSYu1isTlpawfNfdx4iQWm_MXzHPbVpgnYckioxfT2M130_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" .
}