@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE> .
@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:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_head {
  this: np:hasAssertion dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_assertion;
    np:hasProvenance dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_provenance;
    np:hasPublicationInfo dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_publicationInfo;
    a np:Nanopublication .
  
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    a np:PublicationInfo .
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dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_assertion {
  miriam-gene:2108 a ncit:C16612 .
  
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dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_provenance {
  dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_assertion dcterms:description
      "[This review is focused on recent advances about GSDII and its treatment, and the most recent notions about the management and treatment of other metabolic myopathies will be briefly reviewed, including glycogenosis type V (McArdle disease), glycogenosis type III (debrancher enzyme deficiency or Cori disease), CPT-II deficiency, and ETF-dehydrogenase deficiency (also known as riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency or RR-MADD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    prov:wasDerivedFrom dgn-void:befree-2016;
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  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;
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dgn-np:NP1198846.RAfIhzvr7WuZciwgGRuv6DrYu-inJfh9ZSszJiGfmtIQE130_publicationInfo {
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    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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