Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_assertion> ?p ?o ?g. }
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- NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_assertion type Assertion NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_head.
- NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_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." NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_provenance.
- NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_assertion evidence source_evidence_literature NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_provenance.
- NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_assertion SIO_000772 11266688 NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_provenance.
- NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_assertion wasDerivedFrom befree-20140225 NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_provenance.
- NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_assertion wasGeneratedBy ECO_0000203 NP356361.RAkaGyUV0NVGjPPapM2V2XID_ORZ1zUCc_hcUqeh4vlXQ130_provenance.