Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion> ?p ?o ?g. }
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- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion type Assertion NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_head.
- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_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." NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_provenance.
- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion evidence source_evidence_literature NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_provenance.
- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion SIO_000772 24101679 NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_provenance.
- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion wasDerivedFrom befree-20150227 NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_provenance.
- NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_assertion wasGeneratedBy ECO_0000203 NP963639.RAOZrCfgYSobJT3U2VcYdr1Ee9DZY5HAgGOd3BEyTwu0Y130_provenance.