http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#head http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#assertion http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#provenance http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#assertion http://rdf.disgenet.org/resource/gda/DGN658ab5eff562c58503b49e947c8e0c88 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/6323 http://rdf.disgenet.org/resource/gda/DGN658ab5eff562c58503b49e947c8e0c88 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0014550 http://rdf.disgenet.org/resource/gda/DGN658ab5eff562c58503b49e947c8e0c88 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#provenance http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#assertion http://purl.org/dc/terms/description [Typical Severe Myoclonic Epilepsy (SME) and Borderline SME show distinct differences in photoparoxysmal response and gender, which might be caused by some genetic mechanism (s) other than the SCN1A gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#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/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/13129592 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/LHGDN http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/LHGDN http://purl.org/pav/importedOn 2009-03-31 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/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/dc/terms/created 2017-10-17T13:16:04+02:00 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP924155.RAtJ-eBm_3E0CWNUYzKqrPAaORH1SVAw-z8SV8d4ZtVTw 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