@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE> .
@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:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_head {
  this: np:hasAssertion dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_assertion;
    np:hasProvenance dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_provenance;
    np:hasPublicationInfo dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_assertion a np:Assertion .
  
  dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_provenance a np:Provenance .
  
  dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_assertion {
  miriam-gene:6622 a ncit:C16612 .
  
  lld:C0752347 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_provenance {
  dgn-np:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_assertion dcterms:description
      "[These findings suggest that variants in all 3 members of the synuclein gene family, particularly SNCA and SNCG, affect the risk of developing DLBD and warrant further investigation in larger, pathologically defined data sets as well as clinically diagnosed Parkinson disease/dementia with Lewy bodies case-control series.]. 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:20697047;
    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:NP452389.RAKznskEOVVMs76_6lmf0ZAJQqfqAxKyM7IOEtxciZxWE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:29+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}