@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM> .
@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:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_head {
  this: np:hasAssertion dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion;
    np:hasProvenance dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_provenance;
    np:hasPublicationInfo dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion a np:Assertion .
  
  dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_provenance a np:Provenance .
  
  dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion {
  miriam-gene:203228 a ncit:C16612 .
  
  lld:C0242422 a ncit:C7057 .
  
  dgn-gda:DGN0b582b6738ab8fe51a459836a268e0b6 sio:SIO_000628 miriam-gene:203228, lld:C0242422;
    a sio:SIO_001121 .
}

dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_provenance {
  dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion dcterms:description
      "[There is a higher than expected incidence of parkinsonism in ALS patients with C9ORF72 expansions, and the G4C2 repeat has also been reported in other motor phenotypes, such as primary lateral sclerosis, progressive muscular atrophy, corticobasal syndrome and Huntington-like disorders.]. 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:24493408;
    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:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:28+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>,
      <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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}