Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion type Assertion NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_head.
- NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion description "[Mutations of FIG4 are responsible for Yunis-Var�n syndrome, familial epilepsy with polymicrogyria, and Charcot-Marie-Tooth type 4J neuropathy (CMT4J).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_provenance.
- NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion evidence source_evidence_literature NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_provenance.
- NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion SIO_000772 25187576 NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_provenance.
- NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion wasDerivedFrom befree-2016 NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_provenance.
- NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_assertion wasGeneratedBy ECO_0000203 NP1216701.RAekau4ZOyPxmALWzRAhpImyVwvQ5V-maWg3Hj2L--ICo130_provenance.