@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8> .
@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:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_head {
  this: np:hasAssertion dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion;
    np:hasProvenance dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_provenance;
    np:hasPublicationInfo dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion a np:Assertion .
  
  dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_provenance a np:Provenance .
  
  dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion {
  miriam-gene:345651 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN0098e950323713b6e1d5ebbe4153333b sio:SIO_000628 miriam-gene:345651, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_provenance {
  dgn-np:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_assertion dcterms:description
      "[Given that a linkage signal for AAO has been detected near ACT, we hypothesized that ACT genetic variation affects AAO rather than disease risk and this may explain the previous inconsistent findings between ACT genetic variation and AD risk.]. 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:16137793;
    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:NP220775.RABpRf8djoxOl_6lF_kD_pXiweb6cGmufihcaagAZ_Qw8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:02+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" .
}