@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus> .
@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:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_head {
  this: np:hasAssertion dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion;
    np:hasProvenance dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_provenance;
    np:hasPublicationInfo dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion a np:Assertion .
  
  dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_provenance a np:Provenance .
  
  dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion {
  miriam-gene:203228 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGNd994d214af90109b651718d90a17f501 sio:SIO_000628 miriam-gene:203228, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_provenance {
  dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion dcterms:description
      "[This study determined the frequency of C9orf72 repeat expansions in different motor neuron diseases (amyotrophic lateral sclerosis (ALS), motor neuron diseases affecting primarily the first or the second motor neuron and hereditary spastic paraplegia).]. 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:24378086;
    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:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:23+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" .
}