Matches in Nanopublications for { ?s ?p "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- NP720253.RAbI7MCm7H6lJbNYkC4hBcUlaH5v0VFd-7c4ekUKJ9py0130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP720253.RAbI7MCm7H6lJbNYkC4hBcUlaH5v0VFd-7c4ekUKJ9py0130_provenance.
- NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- NP240941.RAr1ZhBlmDvWu2RtG5d4LJN9hVbS-Gkn8CJTGsf_wKJxM130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240941.RAr1ZhBlmDvWu2RtG5d4LJN9hVbS-Gkn8CJTGsf_wKJxM130_provenance.
- NP1322100.RAhwEu3qT_P2tckAFIkMgLvDHqgP-Lb4_cMRY1rw--tPQ130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1322100.RAhwEu3qT_P2tckAFIkMgLvDHqgP-Lb4_cMRY1rw--tPQ130_provenance.
- NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1322104.RAgiWA6-zwkYtLPgJi6P6P4bkzhKqTwxZQ1_C8jT0Es_k130_provenance.
- NP648345.RA0hKwDEczdKSgwewvGt3qv6LZ0w7WYrfaRLoNZkQTHnY130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648345.RA0hKwDEczdKSgwewvGt3qv6LZ0w7WYrfaRLoNZkQTHnY130_provenance.