@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo> .
@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:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_head {
  this: np:hasAssertion dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_assertion;
    np:hasProvenance dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_provenance;
    np:hasPublicationInfo dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_assertion a np:Assertion .
  
  dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_provenance a np:Provenance .
  
  dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_assertion {
  miriam-gene:8914 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
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dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_provenance {
  dgn-np:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_assertion dcterms:description
      "[In addition, SNPs in the ARNTL2, CLOCK, DBP, and TIMELESS genes and haplotypes in the ARNTL, CLOCK, CSNK1E, and TIMELESS genes showed suggestive evidence of association with several circadian phenotypes identified in BP patients.]. 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:18228528;
    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:NP91881.RAcFJyOZlhYXrSA3obk138eV77n7LZE2eqqqCZJZQi8Jo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}