@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U> .
@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:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_head {
  this: np:hasAssertion dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion;
    np:hasProvenance dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_provenance;
    np:hasPublicationInfo dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion a np:Assertion .
  
  dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_provenance a np:Provenance .
  
  dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion {
  miriam-gene:23435 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN66b06cd238c16a7f0587084568934590 sio:SIO_000628 miriam-gene:23435, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_provenance {
  dgn-np:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_assertion dcterms:description
      "[In conclusion, this report contributes to the demonstration of the causative role of the TARDBP gene in ALS pathogenesis and indicates that mutations may affect the stability of the protein even in nonneuronal tissues.]. 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:19224587;
    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:NP166053.RASWGYSw9s4dWf-vd9XPo6EtntiWPagE7FuvU-ugkPw_U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
}