Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion type Assertion NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_head.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion wasGeneratedBy ECO_0000203 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion wasDerivedFrom befree-2016 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion SIO_000772 23163601 NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion evidence source_evidence_literature NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.
- NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_assertion description "[Here we present the algorithm for genetic testing in Serbian patients with demyelinating CMT, based on their genetic specificities: in cases of no PMP22 duplication, and if -X-linked CMT (CMTX) is not contraindicated by pattern of inheritance (male-to-male transmission), one should test for c.94A>G GJB founder mutation, first.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029486.RAb9yFFYCZpvCvXnUlbDykb-IKd1E179DRqMrwgst9tNk130_provenance.