@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_head {
  this: np:hasAssertion dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion;
    np:hasProvenance dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_provenance;
    np:hasPublicationInfo dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion a np:Assertion .
  
  dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_provenance a np:Provenance .
  
  dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion {
  miriam-gene:2629 a ncit:C16612 .
  
  lld:C0752347 a ncit:C7057 .
  
  dgn-gda:DGN0fd0d31d4542a8b9c5ee1740525bad02 sio:SIO_000628 miriam-gene:2629, lld:C0752347;
    a sio:SIO_001121 .
}

dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_provenance {
  dgn-np:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_assertion dcterms:description
      "[Despite the wealth of clinical and genetic evidence supporting the association between mutant genotypes and synucleinopathy risk, the precise mechanisms by which GBA1 mutations lead to PD and DLB remain unclear.]. 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:22327140;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP960252.RA067gqAlHFfi_lRf2vsLwvKju3VoIEYng_wCdTSaetXM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:00+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}