@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI> .
@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:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_head {
  this: np:hasAssertion dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion;
    np:hasProvenance dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_provenance;
    np:hasPublicationInfo dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion a np:Assertion .
  
  dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_provenance a np:Provenance .
  
  dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion {
  miriam-gene:10194 a ncit:C16612 .
  
  lld:C0497327 a ncit:C7057 .
  
  dgn-gda:DGNde1c3ca1cb263650f9ef2916ff45cac3 sio:SIO_000628 miriam-gene:10194, lld:C0497327;
    a sio:SIO_001121 .
}

dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_provenance {
  dgn-np:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_assertion dcterms:description
      "[CAA may contribute to the clinical presentation of dementia by interacting with other neuronal pathologies, leading to more severe cognitive impairment in men with both CAA and AD compared with men with only AD or CAA.]. 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:12058090;
    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:NP836721.RA9nsVi0vUIKe5Snz00HNkVWSC0DP2gm1Jh2-cb7OyjXI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:31+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" .
}