Matches in Nanopublications for { ?s ?p "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP873053.RAomYAWDrM4vdacMfmT5GShuHHfEoRloJifvxHC8nuNbw130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873053.RAomYAWDrM4vdacMfmT5GShuHHfEoRloJifvxHC8nuNbw130_provenance.
- NP303996.RAxLvCLNuv-sV9G-zJ7ZLOOeNbwx4pzG32SjrCX5kAaic130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP303996.RAxLvCLNuv-sV9G-zJ7ZLOOeNbwx4pzG32SjrCX5kAaic130_provenance.
- NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483784.RA1zQj7LWzQfntJSp1VOuQwRjZ0j6O0lpI8m2d5KnPT4c130_provenance.
- NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- NP898256.RAF6h5QRXwGOQUfJi-5JvNYkGW2XtlVrB9_SVwuyTDYzc130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898256.RAF6h5QRXwGOQUfJi-5JvNYkGW2XtlVrB9_SVwuyTDYzc130_provenance.