Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion> ?p ?o ?g. }
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- NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion type Assertion NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_head.
- NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion description "[In the process of screening the above cohort of patients as well as other patients for CMT-causative mutations, we identified several previously unreported mutant alleles: two for connexin 32, three for myelin protein zero, and two for peripheral myelin protein 22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_provenance.
- NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion evidence source_evidence_literature NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_provenance.
- NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion SIO_000772 11835375 NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_provenance.
- NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion wasDerivedFrom gad-20150221 NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_provenance.
- NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_assertion wasGeneratedBy ECO_0000203 NP66423.RApBg81DJTaAyShhW17tbmcZfA9nCcidKDURXN-_mGvbM130_provenance.