@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw> .
@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:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_head {
  this: np:hasAssertion dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_assertion;
    np:hasProvenance dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_provenance;
    np:hasPublicationInfo dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_assertion a np:Assertion .
  
  dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_provenance a np:Provenance .
  
  dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGNbcc9be9f5b21d26caffda253fe9ca655 sio:SIO_000628 miriam-gene:4397, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_provenance {
  dgn-np:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_assertion dcterms:description
      "[Moreover, aberrant DNA methylation and histone modification profiles of discrete DNA sequences, and those at a genome-wide level, have just begun to be described for neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, and Huntington's disease, and in other neurological disorders such as multiple sclerosis, epilepsy, and amyotrophic lateral sclerosis.]. 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:19833297;
    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:NP327382.RAZi8X_Aa2kbAiovzMIvZH2VpMuBiK95bo4F_2CuZDsuw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:11+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" .
}