Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion type Assertion NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_head.
- NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion description "[Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_provenance.
- NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion evidence source_evidence_literature NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_provenance.
- NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion SIO_000772 19158808 NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_provenance.
- NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion wasDerivedFrom befree-2016 NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_provenance.
- NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_assertion wasGeneratedBy ECO_0000203 NP715792.RAbJjKWSZjH_p8hibrIC_SLs0EjF3hxoUtpLXJ5vBtUOo130_provenance.