@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U> .
@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:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_head {
  this: np:hasAssertion dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion;
    np:hasProvenance dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_provenance;
    np:hasPublicationInfo dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion a np:Assertion .
  
  dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_provenance a np:Provenance .
  
  dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0497327 a ncit:C7057 .
  
  dgn-gda:DGNc8b2e511b92aa3802fd2e43c514b97a8 sio:SIO_000628 miriam-gene:4137, lld:C0497327;
    a sio:SIO_001121 .
}

dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_provenance {
  dgn-np:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_assertion dcterms:description
      "[To determine whether functional connectivity is altered in subjects with mutations in the microtubule associated protein tau (MAPT) gene who were asymptomatic but were destined to develop dementia, and to compare these findings to those in subjects with behavioral variant frontotemporal dementia (bvFTD).]. 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:21849646;
    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:NP377535.RAd9YU3Hlve0N5WRLi6lP7Q8RmisB_TnWp48nluE84b9U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:41+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" .
}