@prefix dc: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU> .
@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 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:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_head {
  this: np:hasAssertion dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion;
    np:hasProvenance dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_provenance;
    np:hasPublicationInfo dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion a np:Assertion .
  
  dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_provenance a np:Provenance .
  
  dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  
  lld:C1389280 a ncit:C7057 .
  
  dgn-gda:DGNbb87b96a6688f424154f469d176d262a sio:SIO_000628 miriam-gene:3918, lld:C1389280;
    a sio:SIO_001121 .
}

dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_provenance {
  dgn-np:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_assertion dc:description
      "[The authors report the ninth case of progressive familial encephalopathy in infancy, with calcification of the basal ganglia and chronic cerebrospinal fluid (CSF) lymphocytosis, as recently described by Aicardi and Goutieres.]. 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:3731164;
    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:NP808974.RANNmLWUPxl3uPcgy2HN22lMFARv5FLIMOFcxuNfbGyYU130_publicationInfo {
  this: dc:created "2014-10-02T12:40:16+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}