@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw> .
@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:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_head {
  this: np:hasAssertion dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion;
    np:hasProvenance dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_provenance;
    np:hasPublicationInfo dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion a np:Assertion .
  
  dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_provenance a np:Provenance .
  
  dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion {
  miriam-gene:2629 a ncit:C16612 .
  
  lld:C0752347 a ncit:C7057 .
  
  dgn-gda:DGN2aa6e66cb716498a571011ff27b01a1e sio:SIO_000628 miriam-gene:2629, lld:C0752347;
    a sio:SIO_001121 .
}

dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_provenance {
  dgn-np:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_assertion dcterms:description
      "[Despite the wealth of experimental, clinical and genetic evidence that supports 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:25573151;
    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:NP1253998.RAtutSpnXDbzhKj1R6EaRRkoTOa281WVMaOr_YbMzKLCw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:14+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" .
}