@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_head {
   this: np:hasAssertion dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_assertion ;
    np:hasProvenance dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_provenance ;
    np:hasPublicationInfo dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_provenance a np:Provenance .
  dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_assertion {
   miriam-gene:203228 a ncit:C16612 .
  lld:C0751071 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_provenance {
   dgn-np:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_assertion dcterms:description "[In this Review, we focus on the evidence for, and the approach to, genetic testing in Alzheimer's disease (APP, PSEN1, and PSEN2 genes), frontotemporal dementia (MAPT, GRN, C9ORF72, and other genes), and other familial dementias.]. 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:23927914 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1100636.RALTcVl9Pv-1-9-7BXSGud6zJGu34QgrK_9QSPDezlHKI130_publicationInfo {
   this: dcterms:created "2016-05-13T12:50:05+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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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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}