http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#head http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#assertion http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#provenance http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#assertion http://rdf.disgenet.org/resource/gda/DGN42b67076f09cca4f3c928290a49b0254 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/6324 http://rdf.disgenet.org/resource/gda/DGN42b67076f09cca4f3c928290a49b0254 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0014544 http://rdf.disgenet.org/resource/gda/DGN42b67076f09cca4f3c928290a49b0254 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#provenance http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#assertion http://purl.org/dc/terms/description [To further examine the involvement of homozygous SCN1B mutations in the etiology of Dravet syndrome, we performed mutational analyses on SCN1B in 286 patients with epileptic disorders, including 67 patients with Dravet syndrome who have been negative for SCN1A and SCN2A mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#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/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/23148524 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#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/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/dc/terms/created 2017-10-17T13:16:04+02:00 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP924495.RARIENf4Rf8FmCKM3G5bsYNFRSEllSU0LEyTLbNlUfMxM 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