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- NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_assertion type Assertion NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_head.
- NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_assertion description "[Missense mutations of the GTPase Rab7 cause a dominantly inherited axonal degeneration known as Charcot-Marie-Tooth type 2B through an unknown mechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_provenance.
- NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_assertion evidence source_evidence_literature NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_provenance.
- NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_assertion SIO_000772 20028791 NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_provenance.
- NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_assertion wasDerivedFrom befree-20150227 NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_provenance.
- NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_assertion wasGeneratedBy ECO_0000203 NP985180.RAwqFj3KHUdzMfbc3iA2LWwpJ_B_s2P_9NDdRVB-qx6oQ130_provenance.