@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc> .
@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:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_head {
   this: np:hasAssertion dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_assertion ;
    np:hasProvenance dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_provenance ;
    np:hasPublicationInfo dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_assertion a np:Assertion .
  dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_provenance a np:Provenance .
  dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_assertion {
   miriam-gene:60491 a ncit:C16612 .
  lld:C0013421 a ncit:C7057 .
  dgn-gda:DGN9696d922b195f243a8c9b3e5cafba0b5 sio:SIO_000628 miriam-gene:60491 , lld:C0013421 ;
    a sio:SIO_001121 .
}
dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_provenance {
   dgn-np:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_assertion dcterms:description "[Furthermore, very recently, we found that the GTP cyclohydrolase I gene is causative for hereditary progressive dystonia with marked diurnal fluctuation, also known as DOPA-responsive dystonia (Ichinose, H., Ohye, T., Takahashi, E., Seki, N., Hori, T., Segawa, M., Nomura, Y., Endo, K., Tanaka, H., Tsuji, S., Fujita, K., and Nagatsu, T. (1994) Nature Genetics 8, 236-242).]. 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:7730309 ;
    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:NP510189.RA0NfKPv8Ly6sHsVsBILmTSYavkpOOoHNlhC2JX9WuKQc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:04+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> ;
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}