@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k> .
@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:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_head {
  this: np:hasAssertion dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion;
    np:hasProvenance dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_provenance;
    np:hasPublicationInfo dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion a np:Assertion .
  
  dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_provenance a np:Provenance .
  
  dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion {
  miriam-gene:4287 a ncit:C16612 .
  
  lld:C1839259 a ncit:C7057 .
  
  dgn-gda:DGN428428fea21c427d00cd19628472b11a sio:SIO_000628 miriam-gene:4287, lld:C1839259;
    a sio:SIO_001121 .
}

dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_provenance {
  dgn-np:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_assertion dcterms:description
      "[The size of CAG repeats in the AR gene is one of the determinant factors of the severity and progression rate of SBMA phenotypes, but the meiotic and somatic instability of CAG repeats is far more stable as compared with other diseases caused by trinucleotide repeat expansions such as HD, DRPLA, MJD and SCA1.]. 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:8725492;
    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:NP278110.RA43LGBnt3G_uPa1qOYe9IZyUawqm3vlqXjEqUMAe3M8k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:37+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" .
}