@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY> .
@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:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_head {
  this: np:hasAssertion dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion ;
    np:hasProvenance dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_provenance ;
    np:hasPublicationInfo dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion a np:Assertion .
  dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_provenance a np:Provenance .
  dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion {
  miriam-gene:351 a ncit:C16612 .
  lld:C1842937 a ncit:C7057 .
  dgn-gda:DGN7f3a7eb9e6b74b528e827f94bb7f6095 sio:SIO_000628 miriam-gene:351 , lld:C1842937 ;
    a sio:SIO_001121 .
}
dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_provenance {
  dgn-np:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_assertion dcterms:description "[Although several factors may contribute to CAA in humans, the neuronal origin of transgenic APP, high levels of Abeta in cerebrospinal fluid, and regional localization of CAA in APP23 mice suggest transport and drainage pathways rather than local production or blood uptake of Abeta as a primary mechanism underlying cerebrovascular amyloid formation.]. 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:10570203 ;
    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:NP169970.RAMxB-Ie1iz4DABfYdCe5ygqHSluNp4LylBhh6fJHfrGY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}