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- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion type Assertion NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_head.
- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion description "[Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_provenance.
- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion evidence source_evidence_literature NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_provenance.
- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion SIO_000772 18379723 NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_provenance.
- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion wasDerivedFrom befree-20140225 NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_provenance.
- NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_assertion wasGeneratedBy ECO_0000203 NP524573.RAL0MiCDQSoDO9SMvMmlP1lOQGQ0jlapZfW6YV6l_nKgw130_provenance.