@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM> .
@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/v3.0.0/void/> .

dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_head {
  this: np:hasAssertion dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_assertion;
    np:hasProvenance dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_provenance;
    np:hasPublicationInfo dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_assertion a np:Assertion .
  
  dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_provenance a np:Provenance .
  
  dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0038868 a ncit:C7057 .
  
  dgn-gda:DGNb98efa080448a4bdd43c90850c9817a6 sio:SIO_000628 miriam-gene:4137, lld:C0038868;
    a sio:SIO_001122 .
}

dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_provenance {
  dgn-np:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_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:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP79049.RANvVIqfF5fXQrmOOJzF0fnbe4M_ovaLzShlAOesDZKxM130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:23+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}