Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_assertion> ?p ?o ?g. }
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- NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_assertion type Assertion NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_head.
- NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_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." NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_provenance.
- NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_assertion evidence source_evidence_literature NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_provenance.
- NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_assertion SIO_000772 19158808 NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_provenance.
- NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_assertion wasDerivedFrom befree-20150227 NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_provenance.
- NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_assertion wasGeneratedBy ECO_0000203 NP810426.RAN0e9fmzli6d85ZHQI9LRJ9gmbxnYHQrpKd2j9CAfGhA130_provenance.