@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70> .
@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:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_head {
  this: np:hasAssertion dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion;
    np:hasProvenance dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_provenance;
    np:hasPublicationInfo dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion a np:Assertion .
  
  dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_provenance a np:Provenance .
  
  dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion {
  miriam-gene:4050 a ncit:C16612 .
  
  lld:C0520679 a ncit:C7057 .
  
  dgn-gda:DGN50fa4e23474128cb99567cc504e7ed86 sio:SIO_000628 miriam-gene:4050, lld:C0520679;
    a sio:SIO_001121 .
}

dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_provenance {
  dgn-np:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_assertion dcterms:description
      "[The objective of this study was to to determine the molecular mechanisms of LTB(4) pathway activation in polymorphonuclear cells (PMNs) and early vascular remodeling in OSA and the specific contribution of intermittent hypoxia (IH).]. 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:22761257;
    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:NP237947.RAPF4BvY3xFzSO_cpC-UyKD0vL4A4_TyHISpsuQtE7d70130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}