Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_assertion evidence source_evidence_literature NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_assertion SIO_000772 24101679 NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_assertion wasDerivedFrom befree-20150227 NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_assertion wasGeneratedBy ECO_0000203 NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963530.RAHpNj_dSwzOduOu8E2nWzN6RI5r_2KiAVxjHuU_TVDoM130_provenance.