Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion> ?p ?o ?g. }
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- NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion type Assertion NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_head.
- NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion wasGeneratedBy ECO_0000203 NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_provenance.
- NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion wasDerivedFrom befree-2016 NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_provenance.
- NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion SIO_000772 11254445 NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_provenance.
- NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion evidence source_evidence_literature NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_provenance.
- NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_assertion description "[Although a few candidate disease alleles were identified, the patient survey suggests that SCN1A is not a major contributor to idiopathic generalized epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311295.RAOepgkRY8BPZEJbrEVXrCR85RTxLODhOPdfss5DHv2Mo130_provenance.