http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#head http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#assertion http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#provenance http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#assertion http://rdf.disgenet.org/resource/gda/DGNdffb58ffd02294367ace59df5e56968d http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/3741 http://rdf.disgenet.org/resource/gda/DGNdffb58ffd02294367ace59df5e56968d http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0030443 http://rdf.disgenet.org/resource/gda/DGNdffb58ffd02294367ace59df5e56968d http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#provenance http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#assertion http://purl.org/dc/terms/description [Andersen-Tawil syndrome, a skeletal muscle syndrome associated with periodic paralysis and long QT intervals on the ECG, has been linked to defects in KCNJ2, the gene encoding for the inward rectifier potassium channel (I(K1).)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#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/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/16500306 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#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/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/dc/terms/created 2017-10-17T13:14:05+02:00 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP613635.RAhj89UatQHo40M-0Gnd4cZ5ad8ZvAzU0KCk32DN8xf8s 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