@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY> .
@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:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_head {
  this: np:hasAssertion dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion;
    np:hasProvenance dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_provenance;
    np:hasPublicationInfo dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion a np:Assertion .
  
  dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_provenance a np:Provenance .
  
  dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion {
  miriam-gene:2395 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGNad90ed0b7312048c9749e80549572c30 sio:SIO_000628 miriam-gene:2395, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_provenance {
  dgn-np:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_assertion dcterms:description
      "[The role of genetic background is discussed on the light of the oxidative stress implication, focusing on both complex neurodegenerative diseases (Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis) and monogenic neurological disorders (Huntington's disease, Ataxia telangiectasia, Friedreich Ataxia and others).]. 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:18952194;
    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:NP322302.RApj6MmBLG4HoDWTtRCUAB-uR_aFZ1OH1105kIXs69VeY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:08+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" .
}