Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion type Assertion NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_head.
- NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion description "[Conduction block is unusual in inherited neuropathies, while pupil abnormalities are recognised to occur in CMT especially due to MPZ mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_provenance.
- NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion evidence source_evidence_literature NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_provenance.
- NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion SIO_000772 21256749 NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_provenance.
- NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion wasDerivedFrom befree-20150227 NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_provenance.
- NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_assertion wasGeneratedBy ECO_0000203 NP568337.RA6MWNQYrskQsrBXaEwKny7g0UMFK9dQ3vfKR2vKctv0U130_provenance.