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- source_evidence_literature type ECO_0000212 NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_assertion description "[De novo mutations in SCN1A in sporadic Dravet syndrome and germline mutations in SCN1A, SCN1B, and SCN2A in generalized epilepsies with febrile seizures plus have unraveled the heterogenous myoclonic epilepsies of infancy and early childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_assertion evidence source_evidence_literature NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_assertion SIO_000772 16302874 NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_assertion wasDerivedFrom befree-20150227 NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_assertion wasGeneratedBy ECO_0000203 NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682685.RAMXp-6kVHEVR4lG5botGfsf4Am_qJttNlv_d_tttLcOg130_provenance.