@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU> .
@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:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_head {
  this: np:hasAssertion dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_assertion ;
    np:hasProvenance dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_provenance ;
    np:hasPublicationInfo dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_assertion a np:Assertion .
  dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_provenance a np:Provenance .
  dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_assertion {
  miriam-gene:2629 a ncit:C16612 .
  lld:C0242422 a ncit:C7057 .
  dgn-gda:DGNb6fea3a348ad08f63371e854e83b39df sio:SIO_000628 miriam-gene:2629 , lld:C0242422 ;
    a sio:SIO_001121 .
}
dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_provenance {
  dgn-np:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_assertion dcterms:description "[Recent studies showing an association between glucocerebrosidase deficiency and parkinsonism in Gaucher disease prompted an examination of the glucocerebrosidase gene sequence (GBA) and enzyme activity in brain samples from 57 subjects carrying the diagnosis of Parkinson disease.]. 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:14728994 ;
    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:NP512108.RAf79H3kel4R1UFNyTdwTE7-CJW7kJ6qFy_7o_uppyfwU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:05+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" .
}