@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y> .
@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#> .
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  this: np:hasAssertion dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_assertion ;
    np:hasProvenance dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_provenance ;
    np:hasPublicationInfo dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_provenance a np:Provenance .
  dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_assertion {
  miriam-gene:255022 a ncit:C16612 .
  lld:C0162534 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_provenance {
  dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_assertion dcterms:description "[Since several lines of evidence suggest that AD and prion diseases share pathophysiologic mechanisms, we investigated for the first time the genetic variability of the gene cluster formed by CALHM1 and its paralogs in a series of 235 sporadic Creutzfeldt-Jakob disease (sCJD) patients, and compared the genotypic and allelic frequencies with those presented in 329 controls from the same ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP553859.RAEbGoGYzSn8YcT69uLKTShOqLWf3eJ04bUdXzA698H3Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:34+02:00"^^xsd:dateTime ;
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    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> ;
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