Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion type Assertion NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_head.
- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion wasGeneratedBy ECO_0000203 NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_provenance.
- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion wasDerivedFrom befree-20150227 NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_provenance.
- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion SIO_000772 23163601 NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_provenance.
- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_assertion evidence source_evidence_literature NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_provenance.
- NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_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." NP662171.RAbDG8gT08LA6SiA1RB3yKmlNP7K5xv8WfKnrKeqILeUs130_provenance.