Matches in Nanopublications for { ?s ?p "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP75307.RAJhcqvBsNeIo737D5xyHLg0TqLs4vszI9dsLzrWFd87g130_assertion description "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75307.RAJhcqvBsNeIo737D5xyHLg0TqLs4vszI9dsLzrWFd87g130_provenance.
- NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_assertion description "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499923.RA6uJSHpOKHy2KPGvSdWq9nAPDC1qlRP50Wz-glryJWQo130_provenance.
- assertion description "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_assertion description "[The SSCP technique showed heterozygous defects in the p53 gene in 8 of 39 (20.5%) melanoma tumors: three point mutations in intron sequences (introns 1 and 2) and exon 10, and three new polymorphisms located in introns 1 and 2 (C to T transition at position 11701 in intron 1; C insertion at position 11818 in intron 2; and C insertion at position 11875 in intron 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93527.RAI-7Vf2rWHhWA2YxNmyFx-l_6LGEdoB6hYLgajR1si8A130_provenance.