Matches in Nanopublications for { ?s ?p "[Mutations in the BRCA1/BRCA2 gene confer a substantial increase in breast cancer risk, yet routine clinical genetic screening is limited to the coding regions and intron- exon boundaries, precluding the identification of mutations in noncoding and untranslated regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1231849.RAjr8gedUrujBVM19pwfCGEpZVXoQV-eBmVw0MhmYrY40130_assertion description "[Mutations in the BRCA1/BRCA2 gene confer a substantial increase in breast cancer risk, yet routine clinical genetic screening is limited to the coding regions and intron- exon boundaries, precluding the identification of mutations in noncoding and untranslated regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231849.RAjr8gedUrujBVM19pwfCGEpZVXoQV-eBmVw0MhmYrY40130_provenance.
- NP1231850.RAoMOqUHK9S2yyoS19-DJpbipeYIFR_4BvKkPXNqCGBpU130_assertion description "[Mutations in the BRCA1/BRCA2 gene confer a substantial increase in breast cancer risk, yet routine clinical genetic screening is limited to the coding regions and intron- exon boundaries, precluding the identification of mutations in noncoding and untranslated regions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231850.RAoMOqUHK9S2yyoS19-DJpbipeYIFR_4BvKkPXNqCGBpU130_provenance.