Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion> ?p ?o ?g. }
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- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion type Assertion NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_head.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion description "[To clarify the clinical phenotype and molecular mechanism in X-linked Charcot-Marie-Tooth disease (CMTX) patients with a deletion of the whole connexin 32 (Cx32) coding sequence, we studied a family with this deletion by electrophysiology, Southern blotting and quantitative PCR analyses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion evidence source_evidence_literature NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion SIO_000772 11266688 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion wasDerivedFrom befree-2016 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.
- NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_assertion wasGeneratedBy ECO_0000203 NP312060.RAq9ovhVgoQGAesrUzWAAKcOrh7K4oavTiiEf29HigLes130_provenance.