Matches in Nanopublications for { ?s ?p "[Achondrogenesis type II (Langer-Saldino), caused by a genetic defect in the major cartilage matrix protein, collagen type II, is a rare and severe skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP546621.RAeFKW9NyXaaRPjF9DYXq0_w38xPq5Ay7IfwZIa0OD7GQ130_assertion description "[Achondrogenesis type II (Langer-Saldino), caused by a genetic defect in the major cartilage matrix protein, collagen type II, is a rare and severe skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546621.RAeFKW9NyXaaRPjF9DYXq0_w38xPq5Ay7IfwZIa0OD7GQ130_provenance.
- NP470849.RAe9Cfl8wewnpjClNtG2Pcnuwk5JTlEka9KF4CFyqazm8130_assertion description "[Achondrogenesis type II (Langer-Saldino), caused by a genetic defect in the major cartilage matrix protein, collagen type II, is a rare and severe skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470849.RAe9Cfl8wewnpjClNtG2Pcnuwk5JTlEka9KF4CFyqazm8130_provenance.
- NP470850.RAmFE3qu3Mo5gERrrteZaItke-QZth8JparQ3iRFl9NL0130_assertion description "[Achondrogenesis type II (Langer-Saldino), caused by a genetic defect in the major cartilage matrix protein, collagen type II, is a rare and severe skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470850.RAmFE3qu3Mo5gERrrteZaItke-QZth8JparQ3iRFl9NL0130_provenance.
- NP546615.RAwkgjg7iS5tsCcoymeh3KlaEWaL24zX1S4dYVP-CekMQ130_assertion description "[Achondrogenesis type II (Langer-Saldino), caused by a genetic defect in the major cartilage matrix protein, collagen type II, is a rare and severe skeletal dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546615.RAwkgjg7iS5tsCcoymeh3KlaEWaL24zX1S4dYVP-CekMQ130_provenance.