PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
33851505-6	2021	Here, we summarize these phenotypic variations and report an additional HLTS patient, with a 14-nucleotide de novo duplication in SOX18 and congenital ileal atresia, a feature not previously associated with HLTS.	14-nucleotide	93-106	SRY-box transcription factor 18	Homo sapiens	130-135
8648698-3	1996	We have previously shown that mutagenesis of the nonconsensus src polypyrimidine tract to a 14-nucleotide uninterrupted polypyrimidine tract results in an oversplicing phenotype and a concomitant defective replication in permissive chicken embryo fibroblasts.	14-nucleotide	92-105	SRC proto-oncogene, non-receptor tyrosine kinase	Gallus gallus	62-65
7770051-3	1995	A computer search of the tobacco plastid genome (ptDNA) identified such a putative gRNA, a 14-nucleotide sequence motif that is complementary to the psbL mRNA, including the A nucleotide required to direct the C-to-U change.	14-nucleotide	91-104	PSII reaction center subunit XII	Nicotiana tabacum	149-153
7945383-4	1994	In a gel mobility shift assay, the probe containing the 14-nucleotide recognition sequence formed a complex with the fusion protein and nuclear proteins from Burkitt"s cell lines overexpressing the BCL6 transcripts.	14-nucleotide	56-69	BCL6 transcription repressor	Homo sapiens	198-202
8164672-5	1994	We demonstrate that recombinant FTZ-F1 alpha and FTZ-F1 beta proteins produce similar in vitro DNase I footprint patterns on a 14-nucleotide region of the zebra element and bind to this site with similar affinities and sequence specificities.	14-nucleotide	127-140	ftz transcription factor 1	Drosophila melanogaster	32-44
8164672-5	1994	We demonstrate that recombinant FTZ-F1 alpha and FTZ-F1 beta proteins produce similar in vitro DNase I footprint patterns on a 14-nucleotide region of the zebra element and bind to this site with similar affinities and sequence specificities.	14-nucleotide	127-140	Hormone receptor-like in 39	Drosophila melanogaster	49-60
2824476-12	1987	Matrix plots revealed a 14-nucleotide long repeated sequence (5"-TGAACTTTGAACTT-3") in the 5" nontranscribed region of both genes as well as in a comparable region of another family member that is expressed in enterocytes, cellular retinol binding protein II.	14-nucleotide	24-37	retinol binding protein 2	Homo sapiens	223-258
9630619-8	1998	A 14-nucleotide upstream motif including the atypical TATA box TATAAGAG otherwise occurs only twice in GenBank, in the genes encoding neutrophil elastase and proteinase-3, target proteases inhibited by M/NEI.	14-nucleotide	2-15	serpin family B member 1	Homo sapiens	202-207
35221880-8	2022	Sequencing of ATM exons 48-50 revealed a 14-nucleotide insertion from intron 49, between exons 49 and 50, resulting in premature termination of translation at codon 2439.	14-nucleotide	41-54	ATM serine/threonine kinase	Homo sapiens	14-17
21779925-2	2012	We have solved the NMR structure of a 14-nucleotide hairpin with a novel AUCG tetraloop fold from a Xist A-repeat that is essential for silencing.	14-nucleotide	38-51	X inactive specific transcript	Homo sapiens	100-104
26631803-4	2016	In this case, a frameshift caused by 14-nucleotide duplication in SOX18 appeared de novo resulting in a premature translational stop at the N-terminal region of the central trans-activation domain.	14-nucleotide	37-50	SRY-box transcription factor 18	Homo sapiens	66-71
19336222-1	2009	A novel frameshift mutation attributable to 14-nucleotide insertion in hepatocyte nuclear factor-1alpha (HNF-1alpha) encoding a truncated HNF-1alpha (G554fsX556) with 76-amino acid deletion at its carboxyl terminus was identified in a Thai family with maturity-onset diabetes of the young (MODY).	14-nucleotide	44-57	HNF1 homeobox A	Homo sapiens	71-103
19336222-1	2009	A novel frameshift mutation attributable to 14-nucleotide insertion in hepatocyte nuclear factor-1alpha (HNF-1alpha) encoding a truncated HNF-1alpha (G554fsX556) with 76-amino acid deletion at its carboxyl terminus was identified in a Thai family with maturity-onset diabetes of the young (MODY).	14-nucleotide	44-57	HNF1 homeobox A	Homo sapiens	105-115
19336222-1	2009	A novel frameshift mutation attributable to 14-nucleotide insertion in hepatocyte nuclear factor-1alpha (HNF-1alpha) encoding a truncated HNF-1alpha (G554fsX556) with 76-amino acid deletion at its carboxyl terminus was identified in a Thai family with maturity-onset diabetes of the young (MODY).	14-nucleotide	44-57	HNF1 homeobox A	Homo sapiens	138-148
18621012-4	2008	Furthermore, we discovered an adjacent, second miR-122 binding site, separated from the first by a highly conserved 14-nucleotide sequence.	14-nucleotide	116-129	microRNA 122	Homo sapiens	47-54
16518602-4	2006	We also found that 14-nucleotide deletion in this region of ANK1 which was shifted by five nucleotides in relation to another 14-nucleotide deletion listed in Single Nucleotide Polymorphism National Center for Biotechnology Information (SNP NCBI) database.	14-nucleotide	19-32	ankyrin 1	Homo sapiens	60-64
16518602-4	2006	We also found that 14-nucleotide deletion in this region of ANK1 which was shifted by five nucleotides in relation to another 14-nucleotide deletion listed in Single Nucleotide Polymorphism National Center for Biotechnology Information (SNP NCBI) database.	14-nucleotide	126-139	ankyrin 1	Homo sapiens	60-64