@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s> .
@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:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_head {
  this: np:hasAssertion dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_assertion;
    np:hasProvenance dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_provenance;
    np:hasPublicationInfo dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_assertion a np:Assertion .
  
  dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_provenance a np:Provenance .
  
  dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_assertion {
  miriam-gene:351 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN4d695b82949ffef2577cb1d282279abb sio:SIO_000628 miriam-gene:351, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_provenance {
  dgn-np:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_assertion dcterms:description
      "[In a well-characterized Belgian group of 358 AD patients and 462 controls, we examined whether genetic variability in microRNA (miRNA) binding sites of APP and BACE1 or in associated miRNAs influenced risk for AD.]. 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:19462468;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP48058.RAHVcnWlc-PamsAwTIXRv6gbSBUyraW5dkcooPO70oP1s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}