@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_head { this: np:hasAssertion dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_assertion; np:hasProvenance dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_provenance; np:hasPublicationInfo dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_publicationInfo; a np:Nanopublication . dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_assertion a np:Assertion . dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_provenance a np:Provenance . dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_publicationInfo a np:PublicationInfo . } dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_assertion { miriam-gene:2108 a ncit:C16612 . lld:C1291311 a ncit:C7057 . dgn-gda:DGN651ea7c4bcfd38320ec57c54665206ae sio:SIO_000628 miriam-gene:2108, lld:C1291311; a sio:SIO_001121 . } dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_provenance { dgn-np:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_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; sio:SIO_000772 miriam-pubmed:24997454; 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:NP1198859.RA3nc9DRED_ro5IotKsxi7XVAIjndsTk79K3gURDyynaM130_publicationInfo { this: dcterms:created "2016-05-13T12:50:49+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }