@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs> .
@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:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_head {
  this: np:hasAssertion dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_assertion ;
    np:hasProvenance dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_provenance ;
    np:hasPublicationInfo dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_assertion a np:Assertion .
  dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_provenance a np:Provenance .
  dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_assertion {
  miriam-gene:367 a ncit:C16612 .
  lld:C0234131 a ncit:C7057 .
  dgn-gda:DGN2e843b7c90c87fe2f7d79cec6a136df0 sio:SIO_000628 miriam-gene:367 , lld:C0234131 ;
    a sio:SIO_001121 .
}
dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_provenance {
  dgn-np:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_assertion dcterms:description "[These results suggest that patients with spinal and bulbar muscular atrophy show a slow but steady progression of motor dysfunction over time that is independent of CAG repeat length or clinical phenotype, and that objective outcome measures may be used to evaluate disease severity at an early stage of this 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:22773541 ;
    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:NP531944.RA3aizR3sp2-eT-IfagWj45gsTgoSX-T5_MAOV1PoXLgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:21+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" .
}