Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion> ?p ?o ?g. }
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- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion type Assertion NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_head.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion description "[Mutations in peripheral myelin protein 22 (PMP22) can result in the common peripheral neuropathy Charcot-Marie-Tooth disease (CMTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion evidence source_evidence_literature NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion SIO_000772 21827951 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion wasDerivedFrom befree-2016 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.
- NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_assertion wasGeneratedBy ECO_0000203 NP915767.RACCGQ68NjtxI0O6AMSzbCjXU2hmoVrJZWagRYCQmBiqM130_provenance.