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- source_evidence_literature type ECO_0000212 NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_assertion description "[A literature review of cases with chromosome 2q24.3 deletion revealed that, in most Dravet syndrome cases, it does not involve SCN2A and SCN3A, whereas a complex epilepsy phenotype that is shared with migrating partial seizures of infancy was associated with cases of deletion of the whole sodium channel gene cluster.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_assertion evidence source_evidence_literature NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_assertion SIO_000772 25524840 NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_assertion wasDerivedFrom befree-2016 NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_assertion wasGeneratedBy ECO_0000203 NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249530.RAEhAego6N_kFdyNhE8EYVPOYE5_yyvG8pHdNdJlYPTlA130_provenance.