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- NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_assertion type Assertion NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_head.
- NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_assertion description "[The most common mutations were K790X (19.5%), P664L (6.0%), FH-Tonami-1 (6.0%), IVS15-3C>A (5.5%) and FH-Tonami-2 (4.5%), whereas the other mutations were rare. No apolipoprotein B (apoB) mutations responsible for familial ligand-defective apoB-100 (FDB)]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_provenance.
- NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_assertion evidence source_evidence_literature NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_provenance.
- NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_assertion SIO_000772 12417285 NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_provenance.
- NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_assertion wasDerivedFrom gad-20150221 NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_provenance.
- NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_assertion wasGeneratedBy ECO_0000203 NP65086.RAWeOM3cWmgBFg_OUZDlKcG7syCvSJDhm45At67Tr8HW8130_provenance.