@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE> .
@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:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_head {
  this: np:hasAssertion dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion ;
    np:hasProvenance dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_provenance ;
    np:hasPublicationInfo dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion a np:Assertion .
  dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_provenance a np:Provenance .
  dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion {
  miriam-gene:6992 a ncit:C16612 .
  lld:C0023264 a ncit:C7057 .
  dgn-gda:DGN1e97ad083669fe6b6f339b29dd2e8203 sio:SIO_000628 miriam-gene:6992 , lld:C0023264 ;
    a sio:SIO_001121 .
}
dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_provenance {
  dgn-np:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_assertion dcterms:description "[From clinical evidence these subjects were divided into five groups: (1) necropsy-proved cases of subacute necrotising encephalomyelopathy, (2) cases positive for urinary thiamine pyrophosphate: adenosine triphosphate phosphotransferase inhibitor, (3) clinically likely cases of subacute necrotising encephalomyelopathy (patients still alive, or on whom no necropsy was performed), (4) cases diagnosed as diseases other than subacute necrotising encephalomyelopathy (control group), (5) cases for which no diagnosis had been made.]. 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:7436444 ;
    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:NP563329.RAWHBPVjR5aliL_I4dHB1z9jIlanlf123BrGebTzxQLoE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:39+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" .
}