@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4> .
@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:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_head {
  this: np:hasAssertion dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_assertion;
    np:hasProvenance dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_provenance;
    np:hasPublicationInfo dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_assertion a np:Assertion .
  
  dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_provenance a np:Provenance .
  
  dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_assertion {
  miriam-gene:6311 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGNe674229645f1a8c09b15b88916c3e1b7 sio:SIO_000628 miriam-gene:6311, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_provenance {
  dgn-np:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_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-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:NP193098.RAVZFaK8fvkmvC9_UnhVekjDn-xNmNG_Vd__JBqy1DSG4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:46+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" .
}