Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion type Assertion NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_head.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion description "[Point mutations in the gas3/PMP22 gene account for the dominant inherited peripheral neuropathies Charcot-Marie-Tooth type 1A disease (CMT1A) and Dejerine-Sottas syndrome (DSS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion evidence source_evidence_literature NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion SIO_000772 10982389 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion wasDerivedFrom befree-20150227 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.
- NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_assertion wasGeneratedBy ECO_0000203 NP662211.RASFhpgsK1XaqHKr5vePe71IsmU56GpaILXrHC0P719LY130_provenance.