@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA> .
@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:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_head {
  this: np:hasAssertion dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion;
    np:hasProvenance dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_provenance;
    np:hasPublicationInfo dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion a np:Assertion .
  
  dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_provenance a np:Provenance .
  
  dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0393570 a ncit:C7057 .
  
  dgn-gda:DGNe0e8eb3be536b2c4670417ac47e1a2b7 sio:SIO_000628 miriam-gene:4137, lld:C0393570;
    a sio:SIO_001121 .
}

dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_provenance {
  dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion dcterms:description
      "[We also observed suggestive association between AD and the marker rs9468, which defines the H1 haplotype, an extended haplotype that spans the MAPT gene and has previously been implicated in other neurodegenerative disorders including Parkinson's disease, progressive supranuclear palsy, and corticobasal degeneration.]. 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:22027014;
    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:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}