@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA> .
@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 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:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_head {
  this: np:hasAssertion dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion;
    np:hasProvenance dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance;
    np:hasPublicationInfo dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion a np:Assertion .
  
  dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance a np:Provenance .
  
  dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion {
  miriam-gene:4287 a ncit:C16612 .
  
  lld:C0035258 a ncit:C7057 .
  
  dgn-gda:DGN4c3e319f6ba440e3f33963665f696af5 sio:SIO_000628 miriam-gene:4287, lld:C0035258;
    a sio:SIO_001122 .
}

dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_provenance {
  dgn-np:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_assertion dct:description
      "[To evaluate the contribution of SCA alleles to idiopathic RLS we investigated the CAG repeat length at the SCA1, SCA2, SCA3, SCA6, SCA7, and SCA17 loci in 215 patients who fulfilled the clinical criteria of RLS and presented periodic leg movements in sleep (PLMS) in polysomnographic recording.]. 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:16389595;
    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:NP47937.RAu9OJlu7IOH-b0VpEOOwIwsdwQdV_WiZmL2Dq8wfCnWA130_publicationInfo {
  this: dct:created "2014-10-02T12:32:22+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}