@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg> .
@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/v3.0.0/void/> .
dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_head {
   this: np:hasAssertion dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_assertion ;
    np:hasProvenance dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_provenance ;
    np:hasPublicationInfo dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_assertion a np:Assertion .
  dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_provenance a np:Provenance .
  dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_assertion {
   miriam-gene:773 a ncit:C16612 .
  lld:C0751781 a ncit:C7057 .
  dgn-gda:DGNf74c18a5a901f8b27dee6dce8992309c sio:SIO_000628 miriam-gene:773 , lld:C0751781 ;
    a sio:SIO_001121 .
}
dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_provenance {
   dgn-np:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_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-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP277151.RAoPuB8ZywWWzIAQqgVm0pwh3wxyd9_Bz1J5mEJs46jWg130_publicationInfo {
   this: dcterms:created "2015-08-25T14:40:18+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}