@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg> .
@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:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_head {
  this: np:hasAssertion dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_assertion;
    np:hasProvenance dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_provenance;
    np:hasPublicationInfo dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_assertion a np:Assertion .
  
  dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_provenance a np:Provenance .
  
  dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0349081 a ncit:C7057 .
  
  dgn-gda:DGN849acb2ed001089a7204fc1b98d3205b sio:SIO_000628 miriam-gene:5621, lld:C0349081;
    a sio:SIO_001121 .
}

dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_provenance {
  dgn-np:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_assertion dcterms:description
      "[The combination of dominantly inherited dementia with parkinsonism and extracellular plaques in this distribution that are amyloid and prion protein antibody negative has not been previously reported and thus may represent a new neurological genetic disorder.]. 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:2645825;
    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:NP881562.RAYK4tetiKjYkjb1WsMcwKDmWw8IPlQtEZdKaU5god4hg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:58+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" .
}