@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw> .
@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:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_head {
  this: np:hasAssertion dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_assertion;
    np:hasProvenance dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_provenance;
    np:hasPublicationInfo dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_assertion a np:Assertion .
  
  dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_provenance a np:Provenance .
  
  dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_assertion {
  miriam-gene:3921 a ncit:C16612 .
  
  lld:C0333463 a ncit:C7057 .
  
  dgn-gda:DGNf4913c05b4e2d8f99947825e31a2111a sio:SIO_000628 miriam-gene:3921, lld:C0333463;
    a sio:SIO_001121 .
}

dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_provenance {
  dgn-np:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_assertion dcterms:description
      "[The concordance of NP and NFT pathological change and the discordance of LRP support the concept that, in AD, the former are primarily under genetic control whereas the latter (LRP) is more influenced by disease duration and environmental factors.]. 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:17615170;
    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:NP445059.RATA6v46lPcIFg1bvVL9Bq6EzNnaRDT1CsTuSxATrrERw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:25+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}