@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk> .
@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:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_head {
  this: np:hasAssertion dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion;
    np:hasProvenance dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_provenance;
    np:hasPublicationInfo dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion a np:Assertion .
  
  dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_provenance a np:Provenance .
  
  dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion {
  miriam-gene:1813 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGNf14b4a5b85d0b9c6cd39407fe493962d sio:SIO_000628 miriam-gene:1813, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_provenance {
  dgn-np:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_assertion dcterms:description
      "[XDP has certain similarities to Huntington disease not only in pathological and clinical findings, but also the molecular mechanism, which disturbs expression of genes essential for striatal neurons, such as DRD2.]. 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:16366515;
    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:NP494403.RAJB0MCh7EblVelZRyMikGrr5ApZWjCE6aEsN5VE1TEZk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}