@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo> .
@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:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_head {
  this: np:hasAssertion dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion;
    np:hasProvenance dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_provenance;
    np:hasPublicationInfo dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion a np:Assertion .
  
  dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_provenance a np:Provenance .
  
  dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion {
  miriam-gene:7376 a ncit:C16612 .
  
  lld:C0678236 a ncit:C7057 .
  
  dgn-gda:DGN50e0206cf5629f40a80a9456b9dcaf58 sio:SIO_000628 miriam-gene:7376, lld:C0678236;
    a sio:SIO_001121 .
}

dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_provenance {
  dgn-np:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_assertion dcterms:description
      "[Topics discussed included the natural history and clinical features of the diseases, clinical and laboratory diagnosis of these rare diseases, therapeutic strategies, mouse models of neurodegeneration, molecular analysis of accelerated aging, impact of transcriptional defects and mitochondrial dysfunction on neurodegeneration, and biochemical insights into mechanisms of NER and base excision repair.]. 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:21708183;
    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:NP568245.RAOXeT4JXLdJHvEGYHy2yKSxTl-7WW4166bUKOxYN0RDo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:42+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" .
}