http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#head http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#assertion http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#provenance http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#assertion http://rdf.disgenet.org/resource/gda/DGNba3461b372ada5aefc79812afd8444b6 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/6331 http://rdf.disgenet.org/resource/gda/DGNba3461b372ada5aefc79812afd8444b6 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1142166 http://rdf.disgenet.org/resource/gda/DGNba3461b372ada5aefc79812afd8444b6 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#provenance http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#assertion http://purl.org/dc/terms/description [Mutations in sodium channel alpha-subunit gene (SCN5A) result in multiple arrhythmic syndromes, including long QT3 (LQT3), Brugada syndrome (BS), an inherited cardiac conduction defect, sudden unexpected nocturnal death syndrome (SUNDS) and sudden infant death syndrome (SIDS), constituting a spectrum of disease entities termed Na+ channelopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#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/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/14753626 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#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/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/dc/terms/created 2017-10-17T13:16:05+02:00 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP925972.RA_3AvGmcKKKXgZiBm-14DLwl7bvi6I7NTvWlChFlh2Xw 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