@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q> .
@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:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_head {
  this: np:hasAssertion dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_assertion;
    np:hasProvenance dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_provenance;
    np:hasPublicationInfo dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_assertion a np:Assertion .
  
  dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_provenance a np:Provenance .
  
  dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_assertion {
  miriam-gene:7276 a ncit:C16612 .
  
  lld:C0595905 a ncit:C7057 .
  
  dgn-gda:DGNa7f720407a0d9494d0648a0a27c09a5d sio:SIO_000628 miriam-gene:7276, lld:C0595905;
    a sio:SIO_001121 .
}

dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_provenance {
  dgn-np:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_assertion dcterms:description
      "[Supporting this view are the reduced TTR levels found in CSF of patients with AD, as well as reports of altered TTR expression in the cortex and hippocampus of AD rodent models.]. 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:16698124;
    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:NP891624.RABBNO4Jx39a5klpNGOOYXxlG3_gMZ7d7KoggRi4Nv59Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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" .
}