@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8> .
@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/v4.0.0/void/> .

dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_head {
  this: np:hasAssertion dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_assertion;
    np:hasProvenance dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_provenance;
    np:hasPublicationInfo dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_assertion a np:Assertion .
  
  dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_provenance a np:Provenance .
  
  dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C0236642 a ncit:C7057 .
  
  dgn-gda:DGN8951df4fee06370c2d6c0ccaf61c44f7 sio:SIO_000628 miriam-gene:2896, lld:C0236642;
    a sio:SIO_001121 .
}

dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_provenance {
  dgn-np:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_assertion dcterms:description
      "[PGRN mutations at 17q21 may occur in apparently sporadic frontotemporal lobar dementia with ubiquitinated inclusions cases and in cases presenting with either primary progressive aphasia or the behavioral variant of frontotemporal dementia.]. 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:17522386;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP611503.RAhvfQxZkO3p8QGrbQ2SZcw7QQTF16wf5UfXNkv0iiEL8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:22+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}