@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4> .
@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:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_head {
  this: np:hasAssertion dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_assertion;
    np:hasProvenance dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_provenance;
    np:hasPublicationInfo dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_assertion a np:Assertion .
  
  dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_provenance a np:Provenance .
  
  dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_assertion {
  miriam-gene:203228 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN5f6b86d6d36625b5a5b3afc024b39f60 sio:SIO_000628 miriam-gene:203228, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_provenance {
  dgn-np:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_assertion dcterms:description
      "[To determine the frequency of a hexanucleotide repeat expansion in C9ORF72, a gene of unknown function implicated in frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), in Australian FTD patient cohorts and to examine the clinical and neuropathologic phenotypes associated with this expansion.]. 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:22875086;
    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:NP235986.RAvOc1X3ExEDWS1EQho533bl1450tK406yBS8syL9bbf4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:12+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" .
}