@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A> .
@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:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_head {
   this: np:hasAssertion dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_assertion ;
    np:hasProvenance dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_provenance ;
    np:hasPublicationInfo dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_assertion a np:Assertion .
  dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_provenance a np:Provenance .
  dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_assertion {
   miriam-gene:3778 a ncit:C16612 .
  lld:C0014544 a ncit:C7057 .
  dgn-gda:DGNae53c2423eee93d8a9b257fe4398dff5 sio:SIO_000628 miriam-gene:3778 , lld:C0014544 ;
    a sio:SIO_001121 .
}
dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_provenance {
   dgn-np:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_assertion dcterms:description "[SLO, FLO, SEO, and FEO subgroups did not differ in clinical characteristics such as occurrence of rigidity, hypokinesia, tremor, myoclonus, hallucinations, delusions, or epileptic seizures nor in the profile of deficits on tests assessing memory, language, visuospatial, executive, and praxic functions.]. 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:8614504 ;
    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:NP320409.RALXb_jOzvkmMI5ooDW1kV76HCn8H1Y_jBou2HHdKtY4A130_publicationInfo {
   this: dcterms:created "2014-10-02T12:35:05+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" .
}