@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs> .
@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:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_head {
   this: np:hasAssertion dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_assertion ;
    np:hasProvenance dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_provenance ;
    np:hasPublicationInfo dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_assertion a np:Assertion .
  dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_provenance a np:Provenance .
  dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_assertion {
   miriam-gene:23654 a ncit:C16612 .
  lld:C1852467 a ncit:C7057 .
  dgn-gda:DGN40816ec4ff60b2d0f7b76e7ff08598c1 sio:SIO_000628 miriam-gene:23654 , lld:C1852467 ;
    a sio:SIO_001121 .
}
dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_provenance {
   dgn-np:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_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:NP709757.RAKgFtapIjKDYhtB0Uvah4-szrD77bT_k0V1fbn7mbCcs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:11+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" .
}