@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY> .
@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:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_head {
  this: np:hasAssertion dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_assertion;
    np:hasProvenance dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_provenance;
    np:hasPublicationInfo dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_assertion a np:Assertion .
  
  dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_provenance a np:Provenance .
  
  dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN7f65e704788a088dca0164577f6f6afd sio:SIO_000628 miriam-gene:2521, lld:C0002736;
    a sio:SIO_001122 .
}

dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_provenance {
  dgn-np:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_assertion dcterms:description
      "[The identification of mutations in the TARDBP and more recently the identification of mutations in the FUS gene as the cause of amyotrophic lateral sclerosis (ALS) is providing the field with new insight about the mechanisms involved in this severe neurodegenerative disease.]. 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:19741216;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP156188.RAgfsnggAl_dWGk_PIlplz23BS2vkwhuM-j0EG_hzeRwY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:58+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" .
}