@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA> .
@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:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_head {
  this: np:hasAssertion dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_assertion;
    np:hasProvenance dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_provenance;
    np:hasPublicationInfo dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_assertion a np:Assertion .
  
  dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_provenance a np:Provenance .
  
  dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_assertion {
  miriam-gene:84624 a ncit:C16612 .
  
  lld:C1956346 a ncit:C7057 .
  
  dgn-gda:DGNd871d39e1a5a62e4fb33c79adce6d536 sio:SIO_000628 miriam-gene:84624, lld:C1956346;
    a sio:SIO_001122 .
}

dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_provenance {
  dgn-np:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_assertion dcterms:description
      "[The use of data on genetic variants and the addition of data on global monocytic gene expression led to the identification of the novel functional CAD susceptibility locus LIPA, located on chromosome 10q23.31. The respective eSNPs associated with CAD strongly affect LIPA gene expression level, which was related to endothelial dysfunction, a precursor of CAD.]. 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:21606135;
    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:NP96092.RAoxJy2l6pBsvUi6Bc4BDYyJ8HrajQ7EG4NB5KdgnWaOA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:48+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" .
}