@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc> .
@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 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:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_head {
  this: np:hasAssertion dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion;
    np:hasProvenance dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance;
    np:hasPublicationInfo dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion a np:Assertion .
  
  dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance a np:Provenance .
  
  dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion {
  miriam-gene:2629 a ncit:C16612 .
  
  lld:C0030567 a ncit:C7057 .
  
  dgn-gda:DGN9113925ca19ed0b1aae74439cf460978 sio:SIO_000628 miriam-gene:2629, lld:C0030567;
    a sio:SIO_001122 .
}

dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_provenance {
  dgn-np:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_assertion dct:description
      "[To characterize sequence variation within the glucocerebrosidase (GBA) gene in a select subset of our sample of patients with familial Parkinson disease (PD) and then to test in our full sample whether these sequence variants increased the risk for PD and were associated with an earlier onset of 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:18987351;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP43674.RAo-9b71p3pqlkyBjYZQvziKYn8C1tT2yEsgTekWpKeYc130_publicationInfo {
  this: dct:created "2014-10-02T12:32:20+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}