@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs> .
@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:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_head {
  this: np:hasAssertion dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_assertion;
    np:hasProvenance dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_provenance;
    np:hasPublicationInfo dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_assertion a np:Assertion .
  
  dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_provenance a np:Provenance .
  
  dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C1862939 a ncit:C7057 .
  
  dgn-gda:DGN32bee1ac670813bd8033bbc4957ea739 sio:SIO_000628 miriam-gene:2521, lld:C1862939;
    a sio:SIO_001121 .
}

dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_provenance {
  dgn-np:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_assertion dcterms:description
      "[Mutations in the fused in sarcoma (FUS, also known as translated in liposarcoma) gene have been recently discovered to be associated with familial amyotrophic lateral sclerosis (FALS) in African, European and American populations.]. 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:20224596;
    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:NP799432.RA-Lcubc3ADGJKfCW6CDnYnOG3qbU-g89z3tlUg__pjSs130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:47+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" .
}