@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc> .
@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:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_head {
  this: np:hasAssertion dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_assertion;
    np:hasProvenance dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_provenance;
    np:hasPublicationInfo dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_assertion a np:Assertion .
  
  dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_provenance a np:Provenance .
  
  dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_assertion {
  miriam-gene:9575 a ncit:C16612 .
  
  lld:C0005586 a ncit:C7057 .
  
  dgn-gda:DGN825f138d27b58a84fadc410a1425dc04 sio:SIO_000628 miriam-gene:9575, lld:C0005586;
    a sio:SIO_001122 .
}

dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_provenance {
  dgn-np:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_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:NP46746.RAd_XzIf_xzwighyK-qab6ZG6zALY9nEgjOMyIpYQ-1kc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}