Matches in Nanopublications for { ?s ?p "[Substitution of arginine for leucine at position 569 of the TGFBI gene results in a form of lattice corneal dystrophy that is phenotypically similar to other genetically distinct forms of type I disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Substitution of arginine for leucine at position 569 of the TGFBI gene results in a form of lattice corneal dystrophy that is phenotypically similar to other genetically distinct forms of type I disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP419050.RAzhu0fEFnmpzJTCRUeq8F66MoBxITudXBpLyp13ViBVs130_assertion description "[Substitution of arginine for leucine at position 569 of the TGFBI gene results in a form of lattice corneal dystrophy that is phenotypically similar to other genetically distinct forms of type I disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419050.RAzhu0fEFnmpzJTCRUeq8F66MoBxITudXBpLyp13ViBVs130_provenance.