@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578> .
@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:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_head {
  this: np:hasAssertion dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_assertion;
    np:hasProvenance dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_provenance;
    np:hasPublicationInfo dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_assertion a np:Assertion .
  
  dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_provenance a np:Provenance .
  
  dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_assertion {
  miriam-gene:5621 a ncit:C16612 .
  
  lld:C0162534 a ncit:C7057 .
  
  dgn-gda:DGNa7d1e3cac6f70dc4931b64def713b1b0 sio:SIO_000628 miriam-gene:5621, lld:C0162534;
    a sio:SIO_001121 .
}

dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_provenance {
  dgn-np:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_assertion dcterms:description
      "[This kindred has a unique combination of clinical and neuropathologic features associated with the largest base pair insertion identified to date in PRNP and underscores the need to consider familial prion disease in the differential diagnosis of a familial frontotemporal dementia-like syndrome.]. 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:21911696;
    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:NP923272.RAirhIMYoNj54Ms4SEftLkNbg68mDAIm6zxUBhSVMA578130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:43+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" .
}