@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok> .
@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:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_head {
  this: np:hasAssertion dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion;
    np:hasProvenance dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_provenance;
    np:hasPublicationInfo dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion a np:Assertion .
  
  dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_provenance a np:Provenance .
  
  dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion {
  miriam-gene:79879 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN7fdddf436bb8176009d6a574dcd6f8b7 sio:SIO_000628 miriam-gene:79879, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_provenance {
  dgn-np:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_assertion dcterms: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:NP95661.RAvN1Ek2A1owtMqST5kG19P59qiHwpv_YEm9vdIdK3mok130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}