Matches in Nanopublications for { ?s ?p "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533228.RA99bsa38k2Al-tMmLkSvOiTIG-X0cpVp45TSLLjDDR6w130_provenance.
- NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615218.RAxHGzSRJU4dI2NhYE02QeQKdYj-_Gm_jTq9ovfVwg-iU130_provenance.
- NP842132.RAuLONkgLIWVrMhBm2xuRi873WLZhllNPE0UqxY_t28Mw130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842132.RAuLONkgLIWVrMhBm2xuRi873WLZhllNPE0UqxY_t28Mw130_provenance.
- NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358571.RAtrI_HJTLyj2PYoZk0mA0A8P3DK5EPZN3iroG6M8hH1w130_provenance.
- NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587927.RAPhbIXZQDlZ-duy01lxK9Y7rb5EqDZTAdbVW0rOkFf6A130_provenance.
- NP1358572.RA7mIDvLFrTjvQIBybUusE4i_ONpH1-uzU0jbvuOy1Md8130_assertion description "[Merosin (laminin-2 and -4; alpha 2-beta 1/beta 2-gamma 1) is the predominant laminin variant in skeletal muscle basement membranes; genetic defects affecting its structure or expression are the causes of some types of congenital muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1358572.RA7mIDvLFrTjvQIBybUusE4i_ONpH1-uzU0jbvuOy1Md8130_provenance.