@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY> .
@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:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_head {
  this: np:hasAssertion dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_assertion;
    np:hasProvenance dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_provenance;
    np:hasPublicationInfo dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_assertion a np:Assertion .
  
  dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_provenance a np:Provenance .
  
  dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_assertion {
  miriam-gene:203228 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN8615c9acdaf51e8393878fb0ab018ee4 sio:SIO_000628 miriam-gene:203228, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_provenance {
  dgn-np:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_assertion dcterms:description
      "[Here we show that the large Lund pedigree with behavioral variant of frontotemporal dementia previously described with this disorder has an expansion in the recently described C9ORF72 locus on chromosome 9.]. 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:22483864;
    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:NP181852.RAV6sgiWKtb7I6vQGaWy8ZyrYrtU8y2iPUrYWCCk4epNY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}