@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo> .
@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:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_head {
  this: np:hasAssertion dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_assertion;
    np:hasProvenance dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_provenance;
    np:hasPublicationInfo dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_assertion a np:Assertion .
  
  dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_provenance a np:Provenance .
  
  dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_assertion {
  miriam-gene:120892 a ncit:C16612 .
  
  lld:C0426980 a ncit:C7057 .
  
  dgn-gda:DGN405ee51481ba3b62349d98fed6439fd1 sio:SIO_000628 miriam-gene:120892, lld:C0426980;
    a sio:SIO_001121 .
}

dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_provenance {
  dgn-np:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_assertion dcterms:description
      "[Ten symptomatic LRRK2 patients, 24 sporadic Parkinson's disease patients as well as 10 asymptomatic LRRK2 mutation carriers and 29 matched healthy controls underwent comprehensive clinical assessments with respect to motor and non-motor symptoms.]. 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:21989859;
    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:NP368728.RA6_F_dvvuT8iFlsFkbWGbpXMWDb1Aw6DaP8LzoIF8uDo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:35+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" .
}