@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w> .
@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:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_head {
   this: np:hasAssertion dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_assertion ;
    np:hasProvenance dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_provenance ;
    np:hasPublicationInfo dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_assertion a np:Assertion .
  dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_provenance a np:Provenance .
  dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_assertion {
   miriam-gene:8894 a ncit:C16612 .
  lld:C1858991 a ncit:C7057 .
  dgn-gda:DGN069ab69596817b81dd233f4b8a06f04e sio:SIO_000628 miriam-gene:8894 , lld:C1858991 ;
    a sio:SIO_001122 .
}
dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_provenance {
   dgn-np:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_assertion dcterms:description "[Leukoencephalopathy with vanishing white matter (VWM), also called childhood ataxia with central nervous system hypomyelination (CACH), is an autosomal recessive disease caused by mutations in any of the five genes encoding subunits of the eukaryotic translation initiation factor eIF2B.]. 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:16823698 ;
    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:NP810594.RAjwz6CtrLHoq2CD5ttDK7XZUnJt4GpvtqX1gblPunC9w130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:51+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" .
}