@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg> .
@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:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_head {
  this: np:hasAssertion dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_assertion;
    np:hasProvenance dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_provenance;
    np:hasPublicationInfo dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_assertion a np:Assertion .
  
  dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_provenance a np:Provenance .
  
  dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_assertion {
  miriam-gene:7415 a ncit:C16612 .
  
  lld:C0338451 a ncit:C7057 .
  
  dgn-gda:DGN5053c4e53d05f4a1a3a67cbc5cea1a88 sio:SIO_000628 miriam-gene:7415, lld:C0338451;
    a sio:SIO_001121 .
}

dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_provenance {
  dgn-np:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_assertion dcterms:description
      "[More recently, mutations in the valosin-containing protein (VCP) gene linked to the human genetic disease, Inclusion Body Myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD), were found also to be associated with ALS in some patients.]. 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:22898872;
    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:NP1005779.RAiquCq40XgYOGFQPkBlDORvWuzEvsGAHrOFnclMOgcyg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:21+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" .
}