@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4> .
@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:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_head {
  this: np:hasAssertion dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_assertion;
    np:hasProvenance dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_provenance;
    np:hasPublicationInfo dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_assertion a np:Assertion .
  
  dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_provenance a np:Provenance .
  
  dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_assertion {
  miriam-gene:23583 a ncit:C16612 .
  
  lld:C0276496 a ncit:C7057 .
  
  dgn-gda:DGN324d4e1470fcff959d0af9d06fbd0798 sio:SIO_000628 miriam-gene:23583, lld:C0276496;
    a sio:SIO_001121 .
}

dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_provenance {
  dgn-np:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_assertion dcterms:description
      "[To evaluate the pattern of Pittsburgh Compound B (PiB) retention in subjects with different autosomal dominant mutations associated with familial AD vs that in healthy age-matched control subjects and subjects with probable sporadic AD, to correlate Abeta burden as measured by PiB with available clinical and cognitive data, and to compare the regional brain patterns of PiB retention and fluorodeoxyglucose F 18 (FDG) uptake.]. 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:20008660;
    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:NP390865.RAteRIxlTWWTNChxJ7NEI-ytfiCiLMdiMsYjce1t-vkv4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:53+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" .
}