Matches in Nanopublications for { ?s ?p "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP478381.RAV7apq0pEHPBtVXZt7Si9FG9dgxFOHI1BDWjtq5LNWOo130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478381.RAV7apq0pEHPBtVXZt7Si9FG9dgxFOHI1BDWjtq5LNWOo130_provenance.
- NP665653.RAyACoyz76DbaeTFfTNIcJ9iHwHaCEPjEf0Vfxc84JS6s130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665653.RAyACoyz76DbaeTFfTNIcJ9iHwHaCEPjEf0Vfxc84JS6s130_provenance.
- NP818785.RAwk6mfHLyB_xcAcWAcmOM5WUhOlAZsk5ooNS1atQJjQ0130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP818785.RAwk6mfHLyB_xcAcWAcmOM5WUhOlAZsk5ooNS1atQJjQ0130_provenance.
- NP417246.RAWgWsPWCdiGCTpkohRTBjbAfzOUUj7PZDSji_9xK2AhM130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417246.RAWgWsPWCdiGCTpkohRTBjbAfzOUUj7PZDSji_9xK2AhM130_provenance.
- NP588032.RA7tzkvpW_5iti2WwoPh57zY1bBIg6nQwjinCyr61y0wE130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588032.RA7tzkvpW_5iti2WwoPh57zY1bBIg6nQwjinCyr61y0wE130_provenance.
- NP588440.RA3WA25DR4ndptHQiKzpNYKIMLbgGQ-w3zl0pa_pebjPo130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588440.RA3WA25DR4ndptHQiKzpNYKIMLbgGQ-w3zl0pa_pebjPo130_provenance.
- NP417247.RAxyPiy2zr9borExHGDeV-GXsvADBH97jnqZqwy38EdBc130_assertion description "[A large deletion (1.5 Mb) encompassing the neurofibromatosis type 1 (NF1) gene in a patient with sporadic NF1 associated with dysmorphism, mental retardation, and unusual ocular and skeletal features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP417247.RAxyPiy2zr9borExHGDeV-GXsvADBH97jnqZqwy38EdBc130_provenance.