@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4> .
@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:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_head {
  this: np:hasAssertion dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_assertion;
    np:hasProvenance dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_provenance;
    np:hasPublicationInfo dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_assertion a np:Assertion .
  
  dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_provenance a np:Provenance .
  
  dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0038868 a ncit:C7057 .
  
  dgn-gda:DGN48f00f79b71800715dad49b2de28e34f sio:SIO_000628 miriam-gene:4137, lld:C0038868;
    a sio:SIO_001121 .
}

dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_provenance {
  dgn-np:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_assertion dcterms:description
      "[Previously we have shown that the H1c haplotype on the background of the H1 clade of haplotypes at the MAPT locus is associated with increased risk for progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and Alzheimer's disease (AD).]. 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:17174556;
    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:NP584730.RAvowhpDl2LcZSm322W5QVWVaAE27mq8FbS2BQMDqM6F4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:10+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" .
}