Matches in Nanopublications for { ?s ?p "[high frequency of NRAS codon 61 mutations detected in primary hereditary melanomas may be the result of a hypermutability phenotype associated with a hereditary predisposition for melanoma development in patients with germline CDKN2A mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_assertion description "[high frequency of NRAS codon 61 mutations detected in primary hereditary melanomas may be the result of a hypermutability phenotype associated with a hereditary predisposition for melanoma development in patients with germline CDKN2A mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP118536.RAuD0KRt72eJLqzf1sU5LKx-Q_7xCowc_BFUHqwO11MCY130_provenance.
- NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_assertion description "[high frequency of NRAS codon 61 mutations detected in primary hereditary melanomas may be the result of a hypermutability phenotype associated with a hereditary predisposition for melanoma development in patients with germline CDKN2A mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199952.RADPKTcdqrLCCwUZEcefK36WcSDuHg2sNZvqU183F_CbI130_provenance.
- NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_assertion description "[high frequency of NRAS codon 61 mutations detected in primary hereditary melanomas may be the result of a hypermutability phenotype associated with a hereditary predisposition for melanoma development in patients with germline CDKN2A mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP199951.RAsMqTLUGdHGRjp4QMsXKerwYv2xm_OjDAtCBBajBHZBE130_provenance.