Matches in Nanopublications for { ?s ?p "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367094.RAasbUfHeS3BRO3RLp35CUalLF_lDC5YhZYuHZkpq5hds130_provenance.
- NP367095.RAQMGCAY2TKvT842X0sA9YvLI4GwefJYZIvmkvYnFqCFE130_assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367095.RAQMGCAY2TKvT842X0sA9YvLI4GwefJYZIvmkvYnFqCFE130_provenance.
- NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367092.RAMiuTLH-A4Nfnr0XFxdFuhlbDtah9L0cvT0hempXHQwY130_provenance.
- NP367093.RAHOEj_80AytLhy6NUcOK_sIO2TJm5lYoP5VL6Fki3LxU130_assertion description "[The aim of this study was to characterize eight of the most common reported missense mutations in BRCA1 and BRCA2 occurring in patients tested for hereditary risk of breast and ovarian cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP367093.RAHOEj_80AytLhy6NUcOK_sIO2TJm5lYoP5VL6Fki3LxU130_provenance.