@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8> .
@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:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_head {
  this: np:hasAssertion dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_assertion ;
    np:hasProvenance dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_provenance ;
    np:hasPublicationInfo dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_assertion a np:Assertion .
  dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_provenance a np:Provenance .
  dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_assertion {
  miriam-gene:7415 a ncit:C16612 .
  lld:C0151786 a ncit:C7057 .
  dgn-gda:DGNcda5e5818d86647fe1cbcfdfa69b7144 sio:SIO_000628 miriam-gene:7415 , lld:C0151786 ;
    a sio:SIO_001121 .
}
dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_provenance {
  dgn-np:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_assertion dcterms:description "[Our results elucidate that VCP mutations result in disturbances in several cellular processes, which will help us in the understanding of the pathological mechanisms resulting in muscle weakness and other features of VCP associated 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:19828315 ;
    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:NP687814.RA-yXIfE6cbIyMeUcWjh2SJ4qynsF49z8fbHpatVBkum8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:58+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: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> ;
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}