Matches in Nanopublications for { ?s ?p "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_assertion description "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59229.RAEDIfriEZ78T78raoKUQOezhWYMeYd8rPhNf26U2OKR4130_provenance.
- NP76080.RA6k8cPby5Vp7xWlTrIQjKDc2NkhuYikohSjCs1EIFEH8130_assertion description "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76080.RA6k8cPby5Vp7xWlTrIQjKDc2NkhuYikohSjCs1EIFEH8130_provenance.
- assertion description "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_assertion description "[We conclude that the VHL 598C>T mutation, the most common defect of congenital polycythemia yet found, was spread from a single founder 1,000 to 62,000 years ago.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82439.RAgBlav9wJzy6suarFNo4h8jdspz7Hw_L7gqrbIALv9a0130_provenance.