@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g> .
@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:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_head {
  this: np:hasAssertion dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_assertion ;
    np:hasProvenance dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_provenance ;
    np:hasPublicationInfo dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_assertion a np:Assertion .
  dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_provenance a np:Provenance .
  dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_assertion {
  miriam-gene:10382 a ncit:C16612 .
  lld:C0004936 a ncit:C7057 .
  dgn-gda:DGN2feb0a471cb65793bcad8c443c53d8fe sio:SIO_000628 miriam-gene:10382 , lld:C0004936 ;
    a sio:SIO_001121 .
}
dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_provenance {
  dgn-np:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_assertion dcterms:description "[Moreover, given its allelic association with leukoencephalopathy hypomyelination with atrophy of basal ganglia and cerebellum and protean clinical manifestations (chorea, ataxia, dysarthria, intellectual disability, dysmorphic facial features, and psychiatric disorders), DYT4 should not be categorized as a primary dystonia.]. 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:24598712 ;
    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:NP841770.RADGydkwI3GpGSC-MqOt6Ri1XwKOmrzVF8Sy1WA0jNm3g130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:11+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" .
}