Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion> ?p ?o ?g. }
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- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion type Assertion NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_head.
- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_provenance.
- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion evidence source_evidence_literature NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_provenance.
- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion SIO_000772 10982389 NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_provenance.
- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion wasDerivedFrom befree-20140225 NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_provenance.
- NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_assertion wasGeneratedBy ECO_0000203 NP446392.RAIwNidnUoheDnp_hKEx1tIHqa8ef-D7KRuoqmln7pEOQ130_provenance.