@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w> .
@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 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:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_head {
  this: np:hasAssertion dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_assertion;
    np:hasProvenance dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_provenance;
    np:hasPublicationInfo dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_assertion a np:Assertion .
  
  dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_provenance a np:Provenance .
  
  dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_assertion {
  miriam-gene:10452 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN8d3d726eed960fe5fbcf5f9840181d2b sio:SIO_000628 miriam-gene:10452, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_provenance {
  dgn-np:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_assertion dc:description
      "[In addition to known candidate genes, APOE, TOMM40, and one hypothetical gene LOC100129500 partially overlapping APOE; one novel gene, EPC2, and several other interesting genes were associated with CSF biomarkers that are related to AD. These findings, especially the new EPC2 results, require replication in independent cohorts.]. 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:21123754;
    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:NP78182.RAZW55y9LTCOM8-76dcI69ewANJhj0duXSVFEoxnnkz4w130_publicationInfo {
  this: dc:created "2014-10-02T12:32:38+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}