@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk> .
@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:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_head {
   this: np:hasAssertion dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_assertion ;
    np:hasProvenance dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_provenance ;
    np:hasPublicationInfo dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_assertion a np:Assertion .
  dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_provenance a np:Provenance .
  dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_assertion {
   miriam-gene:10687 a ncit:C16612 .
  lld:C1852467 a ncit:C7057 .
  dgn-gda:DGN13c97a39bbc912ec3ca4d4b7567aaed7 sio:SIO_000628 miriam-gene:10687 , lld:C1852467 ;
    a sio:SIO_001121 .
}
dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_provenance {
   dgn-np:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_assertion dcterms:description "[With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six molecular subtypes (MM1, MM2, MV1, MV2, VV1, and VV2) have been described, which vary with respect to age at disease onset, disease duration, early symptoms, and neuropathology.]. 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:19506221 ;
    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:NP667229.RAINExtAeMicaVMyhVcYJoEqmFncnTXnNMzASRSIKBpsk130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:43+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" .
}