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- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion type Assertion NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_head.
- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion description "[Alpha-1-antitrypsin (A1AT) deficiency is the most common genetic cause of liver disease in children; however, the role of polymorphic heterogeneity in the A1AT gene as a modifier of other forms of pediatric liver disease is not clear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_provenance.
- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion evidence source_evidence_literature NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_provenance.
- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion SIO_000772 17204961 NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_provenance.
- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion wasDerivedFrom befree-2016 NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_provenance.
- NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_assertion wasGeneratedBy ECO_0000203 NP587335.RACIGqiabQyFWO4Bu_caglOp1JRQYUCWJB06SRM0D2b6U130_provenance.