Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_assertion> ?p ?o ?g. }
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- NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_assertion type Assertion NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_head.
- NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_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." NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_provenance.
- NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_assertion evidence source_evidence_literature NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_provenance.
- NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_assertion SIO_000772 19158808 NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_provenance.
- NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_assertion wasDerivedFrom befree-2016 NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_provenance.
- NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_assertion wasGeneratedBy ECO_0000203 NP715793.RAyrBQQaxuGytcI-YD7lxkvJ-2CAfBia4AZKHrIbRzDic130_provenance.