Matches in Nanopublications for { ?s ?p "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_assertion description "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1385024.RAQetN9C6D8SfSM_9yKoCgKIifgJ5aJz5sk9n7X_LNaXo130_provenance.
- NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_assertion description "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.