Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion> ?p ?o ?g. }
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- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion type Assertion NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_head.
- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_provenance.
- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion evidence source_evidence_literature NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_provenance.
- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion SIO_000772 11835375 NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_provenance.
- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion wasDerivedFrom befree-20140225 NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_provenance.
- NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_assertion wasGeneratedBy ECO_0000203 NP853703.RAyTw1hsAipwBxkFoSnGC0fgZ7Ju9hb3LT4nRDjWWbWHA130_provenance.