@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk> .
@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:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_head {
  this: np:hasAssertion dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_assertion;
    np:hasProvenance dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_provenance;
    np:hasPublicationInfo dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_assertion a np:Assertion .
  
  dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_provenance a np:Provenance .
  
  dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_assertion {
  miriam-gene:2896 a ncit:C16612 .
  
  lld:C0236642 a ncit:C7057 .
  
  dgn-gda:DGNfc58d9f4eec5b3e97c7b37e00dc0a66e sio:SIO_000628 miriam-gene:2896, lld:C0236642;
    a sio:SIO_001121 .
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dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_provenance {
  dgn-np:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_assertion dcterms:description
      "[Results revealed: 1) prevalence is approximately 10%, 2) TDP-43 type B and FUS pathologies might have relatively high frequency of psychosis, 3) psychosis in FTD is higher with genetic mutations of C9ORF72 and GRN, 4) imaging researches did not achieve conclusive results, and 5) no treatment for psychosis in FTD is currently available.]. 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:24898651;
    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:NP1188966.RArzY0z-1anELI_Ft5FTzMlRNY4kuX7tiXiOMwuEspgIk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:44+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:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
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    pav:version "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}