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- NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_assertion type Assertion NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_head.
- NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_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." NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_provenance.
- NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_assertion evidence source_evidence_literature NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_provenance.
- NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_assertion SIO_000772 10219749 NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_provenance.
- NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_assertion wasDerivedFrom befree-20140225 NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_provenance.
- NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_assertion wasGeneratedBy ECO_0000203 NP908785.RAJlG6sCqvkK7o4eoYzsyWIQ7V-8ShOfWnkwz1b0aBiBQ130_provenance.