Matches in Nanopublications for { ?s ?p "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 7 of
7
with 100 items per page.
- NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP930560.RA_Nyf_0sRf2OZjynknmIe2tKmWidblt6SyTquYeyRtNs130_provenance.
- NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554980.RALyVHq13cEMyIFycYfwgWH6BC7FGfOFMeYuzXfcba4HU130_provenance.
- NP394588.RAcXY1XNy2z8G5omodHwOXED-_wwsjhKQ-C9M748RXpQg130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394588.RAcXY1XNy2z8G5omodHwOXED-_wwsjhKQ-C9M748RXpQg130_provenance.
- assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP479592.RA8HEUIEExrWmF_ikPKbDfsZ55lcUKAL_HZaO7gN8a6A8130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479592.RA8HEUIEExrWmF_ikPKbDfsZ55lcUKAL_HZaO7gN8a6A8130_provenance.
- NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479600.RAdSccD93QVTiL8o71Lnyv_DtFeqVizsF_MI1G9kMIiEk130_provenance.
- NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_assertion description "[The recent identification of FANCC and FANCG mutations in resected pancreatic tumors selected for loss of heterozygosity on chromosome 9, some of which were present in the germ line DNA, suggests that inactivation of these and other Fanconi complementation group genes may contribute to pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393513.RArVILu9l6IWwjcn4KQOXmQGfIU4w4dzlSMDO508Fwu-s130_provenance.