Matches in Nanopublications for { ?s ?p "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP124296.RAesVryaVP3E9SRWejBVjw2Ndgr2DnGAydOr_bxKC94wU130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124296.RAesVryaVP3E9SRWejBVjw2Ndgr2DnGAydOr_bxKC94wU130_provenance.
- NP168710.RAcLJkLWFOMGexhHKUp7nTclhlKa2zog2ZaOwZWqvvq20130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168710.RAcLJkLWFOMGexhHKUp7nTclhlKa2zog2ZaOwZWqvvq20130_provenance.
- NP168708.RACLkIC5iLZr7aNeR3u9nBrgfBaPkduWxsHY1Y-nGG_2s130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168708.RACLkIC5iLZr7aNeR3u9nBrgfBaPkduWxsHY1Y-nGG_2s130_provenance.
- NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168709.RACmoHZIoomaPOd1hlUdlOaUolVt8ZewTT-3N9ADMd-oQ130_provenance.
- NP149753.RAz7tPkQA1zp2LdS1UzfDc2b49lBFMKJQ7FTjuac0paqs130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149753.RAz7tPkQA1zp2LdS1UzfDc2b49lBFMKJQ7FTjuac0paqs130_provenance.
- NP124423.RANNI3xBdwdBIj05JMI5rUtLBbH-TFEafiiyxfcxeKrbc130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP124423.RANNI3xBdwdBIj05JMI5rUtLBbH-TFEafiiyxfcxeKrbc130_provenance.
- NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149699.RAGLBDurBqTont_Wc4qZvLu3c5r3NinyQQ0eeqYVl2Bp4130_provenance.
- NP168707.RANSRNuCoO4nPGbghJZBLsZs2AgGbWfWsWbHEHLPVKTvE130_assertion description "[Population-based study of BRCA1/2 mutations: family history based criteria identify minority of mutation carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168707.RANSRNuCoO4nPGbghJZBLsZs2AgGbWfWsWbHEHLPVKTvE130_provenance.