@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc> .
@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:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_head {
  this: np:hasAssertion dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_assertion;
    np:hasProvenance dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_provenance;
    np:hasPublicationInfo dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_assertion a np:Assertion .
  
  dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_provenance a np:Provenance .
  
  dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_assertion {
  miriam-gene:6717 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN6ee2efcea9640ccd287e9bbb88bc9c30 sio:SIO_000628 miriam-gene:6717, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_provenance {
  dgn-np:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_assertion dcterms:description
      "[We propose that circadian sleep disturbances are an important pathological feature of HD, that they arise from pathology within the SCN molecular oscillation, and that their treatment will bring appreciable benefits to HD 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:15634777;
    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:NP370480.RAmyOyaCKVTxGr6vepxWS615PoEx2PnkL5Nk_PhkHBpNc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:37+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" .
}