@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs> .
@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:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_head {
  this: np:hasAssertion dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_assertion ;
    np:hasProvenance dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_provenance ;
    np:hasPublicationInfo dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_assertion a np:Assertion .
  dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_provenance a np:Provenance .
  dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  lld:C0595905 a ncit:C7057 .
  dgn-gda:DGN1ca902047ce19ea622edf7bda0fceedf sio:SIO_000628 miriam-gene:4137 , lld:C0595905 ;
    a sio:SIO_001121 .
}
dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_provenance {
  dgn-np:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_assertion dcterms:description "[In order to gain insight into the pathogenesis of frontotemporal lobar degeneration (FTLD), the mean tau load in frontal cortex was compared in 34 patients with frontotemporal dementia linked to chromosome 17 (FTDP-17) with 12 different mutations in the tau gene (MAPT), 11 patients with sporadic FTLD with Pick bodies and 25 patients with early onset Alzheimer's disease (EOAD).]. 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:16866983 ;
    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:NP382035.RA6G-OIykXu6-8dwAq5WtjRhrcpVknbe5M_U4jhp87uYs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:46+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" .
}