Matches in Nanopublications for { ?s ?p "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_provenance.
- NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375261.RAK_QKdQtaeWlKyNIZg__K7HzsAfienPnApF-E-dCxm-w130_provenance.
- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_provenance.
- assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP909534.RA6IkgYs-W_yDfCQspRJQdslFxZqUd86PeQeqK-ZccCLE130_provenance.