Matches in Nanopublications for { ?s ?p "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP792524.RAYjYLghN9FrEIhmkga-Nrnbe_xFB5d6Rwk547upZeUGw130_assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792524.RAYjYLghN9FrEIhmkga-Nrnbe_xFB5d6Rwk547upZeUGw130_provenance.
- assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP792572.RAvjgyNy3S7mn3jirbSkwFxm3OeK_b_Tp029ylvCL0eoE130_assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792572.RAvjgyNy3S7mn3jirbSkwFxm3OeK_b_Tp029ylvCL0eoE130_provenance.
- NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116533.RAEwDVj890L789AAP-e9cF0tiWq1td5IE8ZfiLSpxWlgc130_provenance.
- NP1116539.RAHu2zFX7yeMvpjzZMdio6PiFFeYumNv5xL3ZzgqkOF4Q130_assertion description "[GDF5 is a susceptibility gene for osteoarthritis (OA) and mutations in GDF5 are associated with a wide variety of skeletal malformations ranging from complex syndromes such as acromesomelic chondrodysplasias to isolated forms of brachydactylies or multiple synostoses syndrome 2 (SYNS2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1116539.RAHu2zFX7yeMvpjzZMdio6PiFFeYumNv5xL3ZzgqkOF4Q130_provenance.