@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs> .
@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:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_head {
  this: np:hasAssertion dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_assertion;
    np:hasProvenance dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_provenance;
    np:hasPublicationInfo dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_assertion a np:Assertion .
  
  dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_provenance a np:Provenance .
  
  dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_assertion {
  miriam-gene:79661 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN69362f27b7c24c07cf0416b02f2fe347 sio:SIO_000628 miriam-gene:79661, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_provenance {
  dgn-np:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_assertion dcterms:description
      "[To explore the functional significance of NEIL1, we recently reported that neil1 knock-out and heterozygotic mice develop the majority of symptoms of metabolic syndrome (Vartanian, V., Lowell, B., Minko, I. G., Wood, T. G., Ceci, J. D., George, S., Ballinger, S. W., Corless, C. L., McCullough, A. K., and Lloyd, R. S. (2006) Proc.]. 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:17389588;
    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:NP584093.RAbytyxBH3bualm_pp_VgMhGZrnJ6IJkkL5CF2V1F2QSs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:51+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" .
}