@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c> .
@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:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_head {
  this: np:hasAssertion dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_assertion;
    np:hasProvenance dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_provenance;
    np:hasPublicationInfo dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_assertion a np:Assertion .
  
  dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_provenance a np:Provenance .
  
  dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_assertion {
  miriam-gene:805 a ncit:C16612 .
  
  lld:C0002395 a ncit:C7057 .
  
  dgn-gda:DGN3675f2ac9b98b5f82dddeaa63db75fda sio:SIO_000628 miriam-gene:805, lld:C0002395;
    a sio:SIO_001121 .
}

dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_provenance {
  dgn-np:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_assertion dcterms:description
      "[Our findings provided further evidence on the association between CAM pathway and AD susceptibility, which would be helpful to study the genetic mechanisms of AD and may significantly assist in the development of therapeutic strategies.]. 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:22017384;
    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:NP494593.RABhGHZDOU9rx0HBWO1V7B7BIWCyOacrXu-EMZV3b-B5c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}