Matches in Nanopublications for { ?s ?p "[Cockayne's Syndrome (CS) is a rare autosomal recessive disorder characterized by deficiency in the transcription-couple DNA repair pathway caused by mutations in the genes ERCC6 in 65% of individuals and ERCC8 in 35% of individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Cockayne's Syndrome (CS) is a rare autosomal recessive disorder characterized by deficiency in the transcription-couple DNA repair pathway caused by mutations in the genes ERCC6 in 65% of individuals and ERCC8 in 35% of individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Cockayne's Syndrome (CS) is a rare autosomal recessive disorder characterized by deficiency in the transcription-couple DNA repair pathway caused by mutations in the genes ERCC6 in 65% of individuals and ERCC8 in 35% of individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_assertion description "[Cockayne's Syndrome (CS) is a rare autosomal recessive disorder characterized by deficiency in the transcription-couple DNA repair pathway caused by mutations in the genes ERCC6 in 65% of individuals and ERCC8 in 35% of individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295853.RAT-JUFpQsXxK91nJbS1d5t6XGMIEhpghAj4B1rYHJfCg130_provenance.
- NP1295854.RAO1YIZi294dDcZbG2d5RC5igNm6M0R6MUwaV2s-1fyG4130_assertion description "[Cockayne's Syndrome (CS) is a rare autosomal recessive disorder characterized by deficiency in the transcription-couple DNA repair pathway caused by mutations in the genes ERCC6 in 65% of individuals and ERCC8 in 35% of individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295854.RAO1YIZi294dDcZbG2d5RC5igNm6M0R6MUwaV2s-1fyG4130_provenance.