Matches in Nanopublications for { ?s ?p "[A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP6517.RA8ceTnu-2Ruf3REzjI2IefybzgTCfcYj-ZL0dSabkGeo130_assertion description "[A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6517.RA8ceTnu-2Ruf3REzjI2IefybzgTCfcYj-ZL0dSabkGeo130_provenance.
- assertion description "[A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP419051.RAdiiHHiZPLr6sie0rvsDH4iq-DgaN9hJHssCD4qZmMNw130_assertion description "[A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419051.RAdiiHHiZPLr6sie0rvsDH4iq-DgaN9hJHssCD4qZmMNw130_provenance.
- NP3080.RAu2PvDLdA578zZI-ZYLgFMVfnUx4rlBwkITEkf51Vjso130_assertion description "[A new mutation (Leu569Arg) within exon 13 of the TGFBI (BIGH3) gene causes lattice corneal dystrophy type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3080.RAu2PvDLdA578zZI-ZYLgFMVfnUx4rlBwkITEkf51Vjso130_provenance.