http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#head
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#assertion
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#provenance
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#assertion
http://rdf.disgenet.org/resource/gda/DGNebceb1dd6c5812d96a9cc98fba175eac
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/6331
http://rdf.disgenet.org/resource/gda/DGNebceb1dd6c5812d96a9cc98fba175eac
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C2732979
http://rdf.disgenet.org/resource/gda/DGNebceb1dd6c5812d96a9cc98fba175eac
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#provenance
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#assertion
http://purl.org/dc/terms/description
[Over the past years, hundreds of mutations in SCN5A, the human gene coding for NaV1.5, have been linked to many cardiac electrical disorders, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus syndrome, atrial fibrillation, and dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#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/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/23123192
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#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/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/dc/terms/created
2017-10-17T13:16:05+02:00
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP925437.RATVXCKyAmEyy1bocAT16m9iiCj-5zBCRwQZiJA219pYA
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