Matches in Nanopublications for { ?s ?p "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP937981.RAgVMzQOU20ZwPwk-EUKXa6BDVnvTJJaaFdRSExKSsaBA130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP937981.RAgVMzQOU20ZwPwk-EUKXa6BDVnvTJJaaFdRSExKSsaBA130_provenance.
- NP364898.RAaIRZu_zrR8j_wAZ2fwlqpTod0xQV610cw3iPftdoWwA130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364898.RAaIRZu_zrR8j_wAZ2fwlqpTod0xQV610cw3iPftdoWwA130_provenance.
- assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP435239.RA8arYp9C6yL7cx9jneZ1SNkoTc9EG1BmEiM1dScWBTdo130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435239.RA8arYp9C6yL7cx9jneZ1SNkoTc9EG1BmEiM1dScWBTdo130_provenance.
- assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP319533.RAZNx89_1GNG_RuB-f0YzGgDgFX1A9C_fGbLz_ALz2suU130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319533.RAZNx89_1GNG_RuB-f0YzGgDgFX1A9C_fGbLz_ALz2suU130_provenance.
- NP319398.RAu_-Rpxu9smGFY_6lebD3A55yTJwEGDFy49aIVFJME_I130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319398.RAu_-Rpxu9smGFY_6lebD3A55yTJwEGDFy49aIVFJME_I130_provenance.
- NP900282.RAIYNGsrHK6KdXbOKDJ4rflP_iNwNcI6yvN6Z6MLYzuKw130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900282.RAIYNGsrHK6KdXbOKDJ4rflP_iNwNcI6yvN6Z6MLYzuKw130_provenance.
- NP279803.RAUBkrDtA4_vbylx0Ats6Iv9rxqQc4hbAzOnkyucGEPjQ130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279803.RAUBkrDtA4_vbylx0Ats6Iv9rxqQc4hbAzOnkyucGEPjQ130_provenance.
- NP279805.RAXYcTWkq3n9daafvuZZE_0660OAIH61KGqwPzSVK7OQU130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279805.RAXYcTWkq3n9daafvuZZE_0660OAIH61KGqwPzSVK7OQU130_provenance.
- NP319368.RAD2T0kkiNTgGIjgBXOnYjcKw5rroACRqBFWtDS4u_cCM130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319368.RAD2T0kkiNTgGIjgBXOnYjcKw5rroACRqBFWtDS4u_cCM130_provenance.
- NP279807.RANtNakkR9_6B-9rB1oz9shbkMt3AzysKyhIqMb9Z3dqI130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279807.RANtNakkR9_6B-9rB1oz9shbkMt3AzysKyhIqMb9Z3dqI130_provenance.
- NP279806.RAxQsdwjEDsZ4asJ-JMhAOrNegtY8_-vClGTrTG_EpKqI130_assertion description "[Achondrogenesis II-hypochondrogenesis and severe spondyloepiphyseal dysplasia congenita (SEDC) are lethal forms of dwarfism caused by dominant mutations in the type II collagen gene (COL2A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279806.RAxQsdwjEDsZ4asJ-JMhAOrNegtY8_-vClGTrTG_EpKqI130_provenance.