@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY> .
@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:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_head {
  this: np:hasAssertion dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion ;
    np:hasProvenance dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_provenance ;
    np:hasPublicationInfo dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion a np:Assertion .
  dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_provenance a np:Provenance .
  dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion {
  miriam-gene:404672 a ncit:C16612 .
  lld:C0231341 a ncit:C7057 .
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}
dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_provenance {
  dgn-np:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_assertion dcterms:description "[Studies presented at the workshop described important new insights into the phenotypic complexity of XP, CS and TTD, renewed focus on the neurological manifestations of each of these diseases, as well as keen interest in the role of oxidative stress and mitochondrial dysfunction in neurodegenerative processes and normal and/or premature aging.]. 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:17361460 ;
    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:NP296643.RAOwagKw1FEGMymcUzz84fCC9PPWqeK1AKAtEP9Gv8KVY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}