Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion> ?p ?o ?g. }
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- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion type Assertion NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_head.
- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion description "[X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_provenance.
- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion evidence source_evidence_literature NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_provenance.
- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion SIO_000772 18379723 NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_provenance.
- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion wasDerivedFrom befree-2016 NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_provenance.
- NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_assertion wasGeneratedBy ECO_0000203 NP663248.RANLJxlAXWCwXU4J90tZ3M3jxV7ybx2_WJuHhKwATT_cA130_provenance.