@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0> .
@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/v4.0.0/void/> .
dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_head {
   this: np:hasAssertion dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_assertion ;
    np:hasProvenance dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_provenance ;
    np:hasPublicationInfo dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_provenance a np:Provenance .
  dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_assertion {
   miriam-gene:170302 a ncit:C16612 .
  lld:C0014544 a ncit:C7057 .
  dgn-gda:DGNa3d7024472780166314696c6c6daff94 sio:SIO_000628 miriam-gene:170302 , lld:C0014544 ;
    a sio:SIO_001121 .
}
dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_provenance {
   dgn-np:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_assertion dcterms:description "[We summarize recent updates on the genes and related clinical syndromes involved in the pathogenesis of early-onset epileptic encephalopathies: Aristaless-related homeobox (ARX), cyclin-dependent kinase-like 5 (CDKL5), syntaxin-binding protein 1 (STXBP1), solute carrier family 25 member 22 (SLC25A22), nonerythrocytic α-spectrin-1 (SPTAN1), phospholipase Cβ1 (PLCβ1), membrane-associated guanylate kinase inverted-2 (MAGI2), polynucleotide kinase 3'-phosphatase (PNKP), sodium channel neuronal type 1α subunit (SCN1A), protocadherin 19 (PCDH19), and pyridoxamine 5-prime-phosphate oxidase (PNPO).]. 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:22196487 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP949042.RAgYnSUPKHekRwBIuVemZETOeRwkCcCE9hLbZP7dwuZW0130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:55+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}