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- NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_assertion type Assertion NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_head.
- NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_assertion description "[X-linked Charcot-Marie-Tooth neuropathy (CMTX), which has clinical features similar to CMT1, is associated with mutations in the connexin32 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_provenance.
- NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_assertion evidence source_evidence_literature NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_provenance.
- NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_assertion SIO_000772 10219749 NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_provenance.
- NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_assertion wasDerivedFrom befree-2016 NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_provenance.
- NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_assertion wasGeneratedBy ECO_0000203 NP251190.RAMQARw12i0HVkYBjnxhZ1iRk-E3b4BMYZF5I6b0Fazrs130_provenance.