@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY> .
@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:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_head {
  this: np:hasAssertion dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_assertion;
    np:hasProvenance dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_provenance;
    np:hasPublicationInfo dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_assertion a np:Assertion .
  
  dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_provenance a np:Provenance .
  
  dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_assertion {
  miriam-gene:8398 a ncit:C16612 .
  
  lld:C0393593 a ncit:C7057 .
  
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dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_provenance {
  dgn-np:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_assertion dcterms:description
      "[The present review will describe the parkinsonian phenotypes emerging from the new Mendelian genes which have been linked to PD (such as PARK9 and PARK14), the associated dystonia-parkinsonism disorders (such as the syndromes of neurodegeneration with brain iron accumulation) and the emerging data on heterozygous variants of genes which could influence the risk to develop PD and the PD phenotypes (like PD associated with glucose cerebrosidase mutations).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP177476.RA4urIe0KoIREdJOMD5GX19hSNoTpknrdVRX9KU8VHpZY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:36+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>,
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