@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0> .
@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:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_head {
  this: np:hasAssertion dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_assertion;
    np:hasProvenance dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_provenance;
    np:hasPublicationInfo dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_assertion a np:Assertion .
  
  dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_provenance a np:Provenance .
  
  dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_assertion {
  miriam-gene:55511 a ncit:C16612 .
  
  lld:C0007222 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_provenance {
  dgn-np:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_assertion dcterms:description
      "[Two popular high-throughput gene expression technologies, microarray and Serial Analysis of Gene Expression (SAGE) are capable of producing large amounts of gene expression data with the potential of providing novel insights into fundamental disease processes, especially complex syndromes such as cardiovascular disease, whose etiologies are due to multiple genetic factors and their interplay with the environment.]. 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:12118936;
    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:NP239252.RAfbcCQG0ggyLNpxAtXD12HEE2aMzXGIFHTnywwieo9j0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:14+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;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
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