Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion> ?p ?o ?g. }
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- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion type Assertion NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_head.
- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion description "[the mutation in prothrombin that may have a role in hereditary prothrombin deficiency in Indian patients is named'Prothrombin Vellore 1'and is an Ala362Thr mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_provenance.
- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion evidence source_evidence_literature NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_provenance.
- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion SIO_000772 15892853 NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_provenance.
- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion wasDerivedFrom lhgdn-20090331 NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_provenance.
- NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_assertion wasGeneratedBy ECO_0000203 NP148662.RAnoVT-CfRpYfMO6MLmmAtOiuUyxNbCvLg0rfl6KHwNCo130_provenance.