http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#head http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#provenance http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://rdf.disgenet.org/resource/gda/DGN843d09c90a6fefee49ca798d7f6732b8 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5428 http://rdf.disgenet.org/resource/gda/DGN843d09c90a6fefee49ca798d7f6732b8 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0085605 http://rdf.disgenet.org/resource/gda/DGN843d09c90a6fefee49ca798d7f6732b8 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#provenance http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://purl.org/dc/terms/description [This study emphasizes that genetic testing for POLG mutations in patients with nonsyndromic intractable epilepsies is very important for clinical diagnostics, genetic counseling, and treatment decisions because of the increased risk for VPA-induced liver failure in patients with POLG mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/23448099 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/dc/terms/created 2017-10-17T13:15:31+02:00 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP836807.RAADXK1bQ12zYtF4Yccd_JYz37Qy2x8hXXB4bMF0H4Tqs http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0