@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw> .
@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:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_head {
  this: np:hasAssertion dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_assertion;
    np:hasProvenance dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_provenance;
    np:hasPublicationInfo dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_assertion a np:Assertion .
  
  dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_provenance a np:Provenance .
  
  dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_assertion {
  miriam-gene:6572 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN058d9eaad011a6c70ca7a0e31a443322 sio:SIO_000628 miriam-gene:6572, lld:C0002395;
    a sio:SIO_001122 .
}

dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_provenance {
  dgn-np:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_assertion dcterms:description
      "[The genes encoding choline acetyltransferase (ChAT) and its vesicular transporter (VAChT), CHAT and SLC18A3 respectively, map to the linked region of chromosome 10 and are therefore both positional and obvious functional candidate genes for late-onset 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:12759818;
    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:NP51688.RAafInb1JwRoqQee7DkQoC_ktJG8b0pCFR9hLlzKTRBTw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}