@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw> .
@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/v3.0.0/void/> .

dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_head {
  this: np:hasAssertion dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion;
    np:hasProvenance dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_provenance;
    np:hasPublicationInfo dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion a np:Assertion .
  
  dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_provenance a np:Provenance .
  
  dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion {
  miriam-gene:84894 a ncit:C16612 .
  
  lld:C0270736 a ncit:C7057 .
  
  dgn-gda:DGN815a75c015c688502d7d1efefefc1b24 sio:SIO_000628 miriam-gene:84894, lld:C0270736;
    a sio:SIO_001121 .
}

dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_provenance {
  dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion dcterms:description
      "[In addition, we also investigated the variant in patients with Parkinson disease (PD) because the GWAS LINGO1 variant has been implicated in both ET and PD and etiologic links between the conditions have been suggested.(6.]. 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:23596072;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:25+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}