@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o> .
@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:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_head {
  this: np:hasAssertion dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_assertion;
    np:hasProvenance dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_provenance;
    np:hasPublicationInfo dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_assertion a np:Assertion .
  
  dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_provenance a np:Provenance .
  
  dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_assertion {
  miriam-gene:6314 a ncit:C16612 .
  
  lld:C0035258 a ncit:C7057 .
  
  dgn-gda:DGN007950b837a00dce71f5a84b180e43d7 sio:SIO_000628 miriam-gene:6314, lld:C0035258;
    a sio:SIO_001122 .
}

dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_provenance {
  dgn-np:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_assertion dcterms: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:NP47933.RAVgTiPjryLuCJLFwdYFkIvStqjDfrvvuF9RLlXljwS4o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}