Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP163494.RACGrB7KnUr1oFzPpWD6yQ1xjFS53J4kLNawhr8vRqU9I130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163494.RACGrB7KnUr1oFzPpWD6yQ1xjFS53J4kLNawhr8vRqU9I130_provenance.
• NP15052.RAkDHBnKYsI0we6ERiTaZhTgDABkvUYf2gK7rsZhlK4Pw130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15052.RAkDHBnKYsI0we6ERiTaZhTgDABkvUYf2gK7rsZhlK4Pw130_provenance.
• NP226430.RAHxtbQ8qSZdZn3it1siFCGIT_vto1zwa94LOlTXozuLM130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226430.RAHxtbQ8qSZdZn3it1siFCGIT_vto1zwa94LOlTXozuLM130_provenance.
• NP15050.RA28QZA8lSaA0LgPEKRXajwri-4d1V53hZ-TGdizrcTPw130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15050.RA28QZA8lSaA0LgPEKRXajwri-4d1V53hZ-TGdizrcTPw130_provenance.
• NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP15040.RADCqpKEkGC2lvRoTfLHa7KLvLCG_V-scY5wKe5XKK0xo130_provenance.
• NP225962.RAfu6c7_xhne6ml6OfmpfUS9FqPmx5yYPAEkEkAS7csa0130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225962.RAfu6c7_xhne6ml6OfmpfUS9FqPmx5yYPAEkEkAS7csa0130_provenance.
• NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
• assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP13927.RAQ9zXUsEE7ySFUmL9QP76lHi-uqx4qy1LNdkDNsXkYz8130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13927.RAQ9zXUsEE7ySFUmL9QP76lHi-uqx4qy1LNdkDNsXkYz8130_provenance.
• NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10708.RAR6Z0bJGOa782bLvOsQaVWHl_snQHR6KYl2il_R5P4Jk130_provenance.
• assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332327.RAgvNMNbaWaEtu_SPKGnNBibGw98ZKrQHup3pf9LEMWYs130_provenance.
• NP13925.RAEyPLZQMkfup_YxWKkK6mlyGXql9zd9YNcul4C1aKwpk130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13925.RAEyPLZQMkfup_YxWKkK6mlyGXql9zd9YNcul4C1aKwpk130_provenance.
• NP279512.RApqWAgnBIvxWNi5oMsVG4oAwVN5HspDEzi0BKOnQgzVk130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279512.RApqWAgnBIvxWNi5oMsVG4oAwVN5HspDEzi0BKOnQgzVk130_provenance.
• NP279514.RAnis8vvVhuATXZQ1oq4x_pwjEsinf2-YjdfLWZ6cAOjs130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279514.RAnis8vvVhuATXZQ1oq4x_pwjEsinf2-YjdfLWZ6cAOjs130_provenance.
• NP279516.RAtSdtnmGw58P-TTMYULEQwUZyEx-t_Z9kn0Jm4yHUC7w130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279516.RAtSdtnmGw58P-TTMYULEQwUZyEx-t_Z9kn0Jm4yHUC7w130_provenance.
• NP382876.RAI7aKUL_uYqc3tzh-llHp86ogd7J2wXMIgAaaRvAJC1k130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382876.RAI7aKUL_uYqc3tzh-llHp86ogd7J2wXMIgAaaRvAJC1k130_provenance.
• NP332446.RAJ-g6j1YxHQKDJaBsI4QgQPE2-ZSLLBOXDn5ByCSpT8k130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332446.RAJ-g6j1YxHQKDJaBsI4QgQPE2-ZSLLBOXDn5ByCSpT8k130_provenance.
• NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10707.RAKVyCyeZfe9Q5b9M6_FpwpBRuMlDelGrI06N7EmxYzgs130_provenance.
• NP10709.RA0HLSzBcjY8vtUV7OD9u314XFJHYnfmmY3V8ifT6Cx8c130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10709.RA0HLSzBcjY8vtUV7OD9u314XFJHYnfmmY3V8ifT6Cx8c130_provenance.