Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_assertion type Assertion NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_head.
- NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_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." NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_provenance.
- NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_assertion evidence source_evidence_literature NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_provenance.
- NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_assertion SIO_000772 19158808 NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_provenance.
- NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_assertion wasDerivedFrom befree-20140225 NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_provenance.
- NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_assertion wasGeneratedBy ECO_0000203 NP491492.RALKduyoOKZ_7Hxv-kW4oLWLWJSao7V5ccQNpH4KdcUbA130_provenance.