@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk> .
@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:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_head {
  this: np:hasAssertion dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_assertion;
    np:hasProvenance dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_provenance;
    np:hasPublicationInfo dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_assertion a np:Assertion .
  
  dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_provenance a np:Provenance .
  
  dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_assertion {
  miriam-gene:100380873 a ncit:C16612 .
  
  lld:C0431391 a ncit:C7057 .
  
  dgn-gda:DGNc283e2c84a641765f55331e441c7c67d sio:SIO_000628 miriam-gene:100380873,
      lld:C0431391;
    a sio:SIO_001121 .
}

dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_provenance {
  dgn-np:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_assertion dcterms:description
      "[FCD2 and hemimegalencephaly (HME) may have the same pathogenesis, the principal difference being timing of onset within the 33 mitotic cycles of the periventricular neuroepithelium to exponentially produce the total neuronal population of the cerebral cortex: if the mutation occurs during the late mitotic cycles, FCD2 results as a small dysgenesis; if the mutation occurs in the early mitotic cycles, the distribution of abnormal neurons is more extensive and HME may result.]. 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:25194490;
    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:NP1217553.RApvp0gKZjfuBHqQhWXA8HtUX3kkAGtG713n3adtc4hTk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:58+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}