@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_head {
  this: np:hasAssertion dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_assertion;
    np:hasProvenance dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_provenance;
    np:hasPublicationInfo dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_assertion a np:Assertion .
  
  dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_provenance a np:Provenance .
  
  dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_assertion {
  miriam-gene:348 a ncit:C16612 .
  
  lld:C0242383 a ncit:C7057 .
  
  dgn-gda:DGN710087d7036d3e24e8d991cd53beab67 sio:SIO_000628 miriam-gene:348, lld:C0242383;
    a sio:SIO_001121 .
}

dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_provenance {
  dgn-np:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_assertion dcterms:description
      "[The authors included only the 10,623 control subjects from these studies who were classified as having no evidence of AMD, since variation within the APOE gene has previously been associated with AMD.]. 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:21498624;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP887588.RAVU1_fhty9h6rUNg1FmEDRVBa7OK1dFc7lhEDKUi2Agk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:26+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}