@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM> .
@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:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_head {
  this: np:hasAssertion dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_assertion;
    np:hasProvenance dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_provenance;
    np:hasPublicationInfo dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_assertion a np:Assertion .
  
  dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_provenance a np:Provenance .
  
  dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_assertion {
  miriam-gene:1121 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN347d38e75faf728fc304ba0fb9abff04 sio:SIO_000628 miriam-gene:1121, lld:C0030567;
    a sio:SIO_001121 .
}

dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_provenance {
  dgn-np:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_assertion dcterms:description
      "[These results demonstrate that Rep1 regulates human SNCA expression by enhancing its transcription in the adult nervous system and suggest that homozygosity for the expanded Rep1 allele may mimic locus multiplication, thereby elevating PD risk.]. 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:19498036;
    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:NP270359.RASZc5kj1K7iPcoUunvNnn3LmSel5_VZzeJ46stjN7YIM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:31+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" .
}