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- NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_assertion type Assertion NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_head.
- NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_assertion description "[These results suggest that STX11 gene mutations may be associated with secondary malignancies (MDS/AML), and that there is segregation of specific clinical features in FHL patients with an underlying genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_provenance.
- NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_assertion evidence source_evidence_literature NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_provenance.
- NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_assertion SIO_000772 16582076 NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_provenance.
- NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_assertion wasDerivedFrom befree-20140225 NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_provenance.
- NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_assertion wasGeneratedBy ECO_0000203 NP722713.RAA9yLKfTSHa0PyUYDmfRuiaDrWlI5dOnA3w4jNz12Qtk130_provenance.