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- source_evidence_literature type ECO_0000212 NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- befree-2016 importedOn "2016-02-19" NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_assertion wasGeneratedBy ECO_0000203 NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_assertion wasDerivedFrom befree-2016 NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_assertion SIO_000772 21248271 NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_assertion evidence source_evidence_literature NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.
- NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_assertion description "[Most mutations in SCN1A-related epilepsies are novel and when an infant presents with febrile seizures (FS) it is uncertain if they will have simple FS, FS+, or develop a severe epilepsy such as Dravet syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP866374.RAD1ZO-YddUHwrY76HMVDTRjls0qNoDq9RswHsV749wW8130_provenance.