@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU> .
@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:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_head {
  this: np:hasAssertion dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_assertion;
    np:hasProvenance dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_provenance;
    np:hasPublicationInfo dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_provenance a np:Provenance .
  
  dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_assertion {
  miriam-gene:28954 a ncit:C16612 .
  
  lld:C0004352 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_provenance {
  dgn-np:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_assertion dcterms:description
      "[Using lentiviral gene transfer, microarray and Q-RT-PCR technologies, we identify rs2670660 allele-specific gene expression signatures (GES) which appear useful for detecting the activated states of innate immunity/inflammasome pathways in approximately 700 clinical samples from 185 control subjects and 350 patients diagnosed with nine common human disorders, including Crohn's disease, ulcerative colitis, rheumatoid arthritis, Huntington disease, autism, Alzheimer disease, obesity, prostate and breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP408720.RADhm_4mB92z85CLFgIVxgBxPnYwvEpc07mNiWU5QTuVU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:03+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
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    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>;
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