@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o> .
@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:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_head {
   this: np:hasAssertion dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_assertion ;
    np:hasProvenance dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_provenance ;
    np:hasPublicationInfo dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_assertion a np:Assertion .
  dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_provenance a np:Provenance .
  dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_assertion {
   miriam-gene:4137 a ncit:C16612 .
  lld:C0524851 a ncit:C7057 .
  dgn-gda:DGNdc8208ee1845cf3cbab309891749517d sio:SIO_000628 miriam-gene:4137 , lld:C0524851 ;
    a sio:SIO_001121 .
}
dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_provenance {
   dgn-np:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_assertion dcterms:description "[Recent studies have detected an over-representation of the H1 haplotype of the MAPT gene in neurodegenerative disorders such as progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), frontotemporal dementia (FTD) and Parkinson's disease (PD), whereas the H2 haplotype has been found to be related to familial FTD.]. 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:18854867 ;
    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:NP697893.RAONLuYW0Gzzsm72XMoyQP-RFiJLBm8ShFsqyLHCl926o130_publicationInfo {
   this: dcterms:created "2016-05-13T12:47:01+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" .
}