@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg> .
@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:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_head {
  this: np:hasAssertion dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion;
    np:hasProvenance dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_provenance;
    np:hasPublicationInfo dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion a np:Assertion .
  
  dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_provenance a np:Provenance .
  
  dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion {
  miriam-gene:7415 a ncit:C16612 .
  
  lld:C1368019 a ncit:C7057 .
  
  dgn-gda:DGNfebb6eb712252096ecbc3a70ef3335ea sio:SIO_000628 miriam-gene:7415, lld:C1368019;
    a sio:SIO_001121 .
}

dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_provenance {
  dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion dcterms:description
      "[Mutations in valosin-containing protein (VCP) gene, already known to be associated with the multisystemic disorder, inclusion body myopathy with Paget's disease and frontotemporal dementia (IBMPFD), have been recently found also in familial cases of amyotrophic lateral sclerosis (ALS).]. 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:22137929;
    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:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:35+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" .
}