@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc> .
@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:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_head {
  this: np:hasAssertion dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_assertion;
    np:hasProvenance dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_provenance;
    np:hasPublicationInfo dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_assertion a np:Assertion .
  
  dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_provenance a np:Provenance .
  
  dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_assertion {
  miriam-gene:2521 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGN89ce317cd29e4a3bd1c1c1abc6089667 sio:SIO_000628 miriam-gene:2521, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_provenance {
  dgn-np:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_assertion dcterms:description
      "[The degeneration spread over multiple systems might be caused not only by the appearance of the FUS immunoreactive neuronal cytoplasmic inclusions but also by the degeneration of neuronal connections from the primary motor cortex and related areas.]. 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:22980027;
    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:NP527317.RAFuB7MaetE0f1EA-xZG3yI6Bo6InSBy584AVVWsYx0tc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:16+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" .
}