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- NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_assertion type Assertion NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_head.
- NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_assertion description "[ALG8 splice site mutations and missense mutations causing ALG8 deficiency in patients with congenital disorders of glycosylation type Ih.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_provenance.
- NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_assertion evidence source_evidence_literature NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_provenance.
- NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_assertion SIO_000772 15235028 NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_provenance.
- NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_assertion wasDerivedFrom lhgdn-20090331 NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_provenance.
- NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_assertion wasGeneratedBy ECO_0000203 NP205780.RAdQUZ-EY6CznwNbIuJwqm6AjyjRNsS1VOVo5pfXdTeVA130_provenance.