@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE> .
@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:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_head {
  this: np:hasAssertion dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_assertion;
    np:hasProvenance dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_provenance;
    np:hasPublicationInfo dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_assertion a np:Assertion .
  
  dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_provenance a np:Provenance .
  
  dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_assertion {
  miriam-gene:5132 a ncit:C16612 .
  
  lld:C1869117 a ncit:C7057 .
  
  dgn-gda:DGN1dd625bd8ca6ace21c8594c8d32b40ce sio:SIO_000628 miriam-gene:5132, lld:C1869117;
    a sio:SIO_001121 .
}

dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_provenance {
  dgn-np:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_assertion dcterms:description
      "[Identifying the PDC locus on chromosome 2q will facilitate discovery of the PDC gene and enable investigators to determine whether PDC is genetically homogeneous and whether other paroxysmal movement disorders are also genetically linked to the PDC locus.]. 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:8659518;
    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:NP856897.RAwy_vG9HbLSo5oBGs2r302CWZFFJ16DjCOZPTJ1i52sE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}