@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM> .
@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:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_head {
  this: np:hasAssertion dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_assertion;
    np:hasProvenance dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_provenance;
    np:hasPublicationInfo dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_assertion a np:Assertion .
  
  dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_provenance a np:Provenance .
  
  dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_assertion {
  miriam-gene:3133 a ncit:C16612 .
  
  lld:C0243026 a ncit:C7057 .
  
  dgn-gda:DGN6e59ccb5101471c801d38404b4ed6088 sio:SIO_000628 miriam-gene:3133, lld:C0243026;
    a sio:SIO_001121 .
}

dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_provenance {
  dgn-np:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_assertion dcterms:description
      "[The prognostic significance of abnormal, early polymorphonuclear leukocyte (PMNL) activation in the development of sepsis, high neutrophil expression of certain receptor molecules, low monocyte and lymphocyte expression of major histocompatibility antigen MHC-class II, and the influence of the genetically encoded TNF and IL-1 secretion on the course of the illness are discussed and related to ANP.]. 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:7806909;
    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:NP680588.RAmvvb86rzww93Gop4B-KwpL0b4uG4-43XvxsyUgwx6HM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:50+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" .
}