@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ> .
@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/v3.0.0/void/> .

dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_head {
  this: np:hasAssertion dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_assertion;
    np:hasProvenance dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_provenance;
    np:hasPublicationInfo dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_assertion a np:Assertion .
  
  dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_provenance a np:Provenance .
  
  dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGN45babaeccec3e06cab7e91fec779c6ec sio:SIO_000628 miriam-gene:2896, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_provenance {
  dgn-np:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_assertion dcterms:description
      "[Mutations in the microtubule associated protein tau (MAPT) and progranulin (PGRN) have been identified in several neurodegenerative disorders, such as frontotemporal lobar degeneration (FTLD), progressive supranuclear palsy (PSP), and corticobasal syndrome (CBS).]. 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:22818528;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP434152.RAITAFHQpi_PMaPfAyUhbKEJPI1ibpk22tH4DLhwYVVGQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:53+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}