@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM> .
@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:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_head {
  this: np:hasAssertion dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_assertion;
    np:hasProvenance dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_provenance;
    np:hasPublicationInfo dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_assertion a np:Assertion .
  
  dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_provenance a np:Provenance .
  
  dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_assertion {
  miriam-gene:10667 a ncit:C16612 .
  
  lld:C0205710 a ncit:C7057 .
  
  dgn-gda:DGN06ee1b4bfdbccf4c769c27687ad851c9 sio:SIO_000628 miriam-gene:10667, lld:C0205710;
    a sio:SIO_001121 .
}

dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_provenance {
  dgn-np:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_assertion dcterms:description
      "[Clinical features, including postnatal onset, catastrophic epilepsy, lactic acidemia, early lethality and neuroimaging findings of the patients with FARS2 variants, resembled each other closely, and neuropathology was consistent with Alpers syndrome.]. 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:22833457;
    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:NP402220.RArbcCfdO5DxgIt7yVYKtT3ViYvwIbRUftJZLUv8zJvJM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:59+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" .
}