@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs> .
@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:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_head {
   this: np:hasAssertion dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_assertion ;
    np:hasProvenance dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_provenance ;
    np:hasPublicationInfo dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_assertion a np:Assertion .
  dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_provenance a np:Provenance .
  dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_assertion {
   miriam-gene:6314 a ncit:C16612 .
  lld:C0020179 a ncit:C7057 .
  dgn-gda:DGNfa510801357028dedb3be0d226794441 sio:SIO_000628 miriam-gene:6314 , lld:C0020179 ;
    a sio:SIO_001121 .
}
dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_provenance {
   dgn-np:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_assertion dcterms:description "[Recently, the transglutaminase activity has been hypothesized to be involved in the pathogenetic mechanisms responsible for the formation of cellular inclusions present in Huntington disease and in all the other polyglutamine (polyQ) diseases hitherto identified, such as spinobulbar muscular atrophy or Kennedy disease, spinocerebellar ataxias (SCA-1, SCA-2, SCA-3 or Machado-Joseph disease, SCA-6 and SCA-7) and dentatorubropallidoluysian atrophy.]. 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:11719247 ;
    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:NP337130.RABlaenX7s_Nc0S2Ne7D4eXzoECyUs6o8TqiCpmRaqPBs130_publicationInfo {
   this: dcterms:created "2016-05-13T12:44:18+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" .
}