Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP483331.RAr1LWQ1jpQdMi-K4p8KSZP0I5fKqeDxltWZN6kjzlFbc130_provenance.
• NP734818.RAnpLZjO4Ro2qdCu8ROPOrdc_RfrKHNocsX_8pkI5kjn4130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734818.RAnpLZjO4Ro2qdCu8ROPOrdc_RfrKHNocsX_8pkI5kjn4130_provenance.
• NP593177.RAXHa3CrI2-FncROcWx07AVox8sJwQnP4AXHJBxWO4fqU130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593177.RAXHa3CrI2-FncROcWx07AVox8sJwQnP4AXHJBxWO4fqU130_provenance.
• NP748020.RAcvIdo9t-PQlkDpveQ5Tz2m6mI_KMYNj-J5_HMwoiVpY130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP748020.RAcvIdo9t-PQlkDpveQ5Tz2m6mI_KMYNj-J5_HMwoiVpY130_provenance.
• NP192619.RA8-I_O3QaUFyWEou2ggHm33sthq_UrdrYsSym79i2llY130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192619.RA8-I_O3QaUFyWEou2ggHm33sthq_UrdrYsSym79i2llY130_provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP783119.RA87CO1fhaG44VtVgzFhHqV2kXf9pI9b3zTv9sQApVdkY130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783119.RA87CO1fhaG44VtVgzFhHqV2kXf9pI9b3zTv9sQApVdkY130_provenance.
• NP912465.RA5jXiCCDj1BXrJCHX0L_fK2aW0UaoKHRa56ZQGHwubws130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912465.RA5jXiCCDj1BXrJCHX0L_fK2aW0UaoKHRa56ZQGHwubws130_provenance.
• NP320366.RATE1dQPoJ06HlJ5jjKvP23DZXfZXc5OIHCCCP8y1dgv4130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320366.RATE1dQPoJ06HlJ5jjKvP23DZXfZXc5OIHCCCP8y1dgv4130_provenance.
• NP320396.RAbO55BLMDvlkjuKC4RkSaXC4YZ44tNL_yb59OMy6JGck130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320396.RAbO55BLMDvlkjuKC4RkSaXC4YZ44tNL_yb59OMy6JGck130_provenance.
• NP320368.RAiefJadVKdSl7_EAm536oQn7PaiPIwYFIo3CGELrVP5Y130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320368.RAiefJadVKdSl7_EAm536oQn7PaiPIwYFIo3CGELrVP5Y130_provenance.
• NP400416.RASCuFmNMJuk-uY_oK8Nl13WwbrhB96DiS8KghblbGQuY130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400416.RASCuFmNMJuk-uY_oK8Nl13WwbrhB96DiS8KghblbGQuY130_provenance.
• NP400418.RASFeMyzTpDqM7j1HtTtW78VFOUT9kizwO58LnRIxPxmo130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400418.RASFeMyzTpDqM7j1HtTtW78VFOUT9kizwO58LnRIxPxmo130_provenance.
• NP400421.RAdgfgLS51p2muMHvE1mB6nC-QWBGP6LEzpYhBnyKv_Qs130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400421.RAdgfgLS51p2muMHvE1mB6nC-QWBGP6LEzpYhBnyKv_Qs130_provenance.
• NP400417.RAutATB_y2fXZZcw00mTdNU8JXdhNsz_Bu_vAMaxbVWFM130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400417.RAutATB_y2fXZZcw00mTdNU8JXdhNsz_Bu_vAMaxbVWFM130_provenance.
• NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320406.RA7ma9-KM2gRnXkcsIoh4MRZhN7b0HM_sH-r45AyJgoig130_provenance.
• NP320409.RA874mBM3RNScY89VAdDXCJr9jKbmOBtD0kmzXeS_y6pM130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320409.RA874mBM3RNScY89VAdDXCJr9jKbmOBtD0kmzXeS_y6pM130_provenance.
• NP320353.RAPCrQ8aK3sgGLOzbE3rcnSgco2hM7OKOQu-8jO2VEYsA130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320353.RAPCrQ8aK3sgGLOzbE3rcnSgco2hM7OKOQu-8jO2VEYsA130_provenance.
• NP400414.RAMZMzPUzyNbEptYsAmL0i4SU7g3RpnnxEDORqE1a4f9U130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400414.RAMZMzPUzyNbEptYsAmL0i4SU7g3RpnnxEDORqE1a4f9U130_provenance.
• NP400415.RAEsCTNoEyUcdmlnVQ5-SAsNxD3pdsrUsF8Kx5IUR_FSA130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400415.RAEsCTNoEyUcdmlnVQ5-SAsNxD3pdsrUsF8Kx5IUR_FSA130_provenance.
• NP400419.RAFfJAmhWWIYolLYAioTPrVlMiX_ZJL7rG9VE3q3UWXhM130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400419.RAFfJAmhWWIYolLYAioTPrVlMiX_ZJL7rG9VE3q3UWXhM130_provenance.
• NP400420.RAI9tYz7SIUTk78PbqF_mjCd-xUrYG5ZYZfGVWAi65yG0130_assertion description "[Recessive mutations in two of the three collagen VI genes, COL6A2 and COL6A3, have recently been shown to cause Ullrich congenital muscular dystrophy (UCMD), a frequently severe disorder characterized by congenital muscle weakness with joint contractures and coexisting distal joint hyperlaxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400420.RAI9tYz7SIUTk78PbqF_mjCd-xUrYG5ZYZfGVWAi65yG0130_provenance.