Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_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." NP820593.RAcb_ByrU3VOXzZK84FWDEYHNrXtwy2UraQ4OxPh38KJQ130_provenance.
- 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.
- NP436133.RAGmQFdbWPlch7skt12SHq0FXuy_COtTFo0dVAL87pIXA130_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." NP436133.RAGmQFdbWPlch7skt12SHq0FXuy_COtTFo0dVAL87pIXA130_provenance.
- 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." provenance.
- NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_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." NP801796.RAO4g5vL0oJPisSI3htFL2zLrQcqoYw009zZCMVbdaAU0130_provenance.