Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion> ?p ?o ?g. }
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- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion type Assertion NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_head.
- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion description "[Despite a growing body of evidence concerning the gene structures responsible for genetically heterogenous CMT2B and other CMT2 neuropathies, little is known about the in vitro neuropathy model and how CMT2B-associated mutation-caused aberrant neuritogenesis is properly reversed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_provenance.
- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion evidence source_evidence_literature NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_provenance.
- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion SIO_000772 20645406 NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_provenance.
- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion wasDerivedFrom befree-20140225 NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_provenance.
- NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_assertion wasGeneratedBy ECO_0000203 NP756384.RAYpn8dERsdfImMqyGEDcHIVnIPCn0xQGc7gs6oUYKJyQ130_provenance.