@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI> .
@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:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_head {
  this: np:hasAssertion dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion;
    np:hasProvenance dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_provenance;
    np:hasPublicationInfo dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion a np:Assertion .
  
  dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_provenance a np:Provenance .
  
  dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGNb2f079b409d9b5b1e1a7bf572c9f0778 sio:SIO_000628 miriam-gene:4137, lld:C0338451;
    a sio:SIO_001122 .
}

dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_provenance {
  dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion dcterms:description
      "[ This study of the largest series of patients with FTD confirms the primary role of tau in FTD and establishes that the H1 haplotype of the tau gene and the E2 allele of APOE interact by an unknown mechanism that increases the risk of 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:12056929;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:29+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" .
}