@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus> .
@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:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_head {
  this: np:hasAssertion dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion;
    np:hasProvenance dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_provenance;
    np:hasPublicationInfo dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion a np:Assertion .
  
  dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_provenance a np:Provenance .
  
  dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion {
  miriam-gene:4137 a ncit:C16612 .
  
  lld:C0393570 a ncit:C7057 .
  
  dgn-gda:DGN9c5b092b94af479aeec7a313944cf90a sio:SIO_000628 miriam-gene:4137, lld:C0393570;
    a sio:SIO_001121 .
}

dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_provenance {
  dgn-np:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_assertion dcterms:description
      "[The MAPT (microtubule-associated protein tau) locus is one of the most remarkable in neurogenetics due not only to its involvement in multiple neurodegenerative disorders, including progressive supranuclear palsy, corticobasal degeneration, Parksinson's disease and possibly Alzheimer's disease, but also due its genetic evolution and complex alternative splicing features which are, to some extent, linked and so all the more intriguing.]. 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:22723018;
    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:NP286686.RALYTEucMU6n_C5Hig3leNTc4wdM_-EBP0h7aRFW9Pjus130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:43+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" .
}