Matches in Nanopublications for { ?s ?p "[Mutations in vascular endothelial growth factor (VEGF) receptor-3 (VEGFR3 or FLT4) cause Milroy disease, an autosomal dominant condition that presents with congenital lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP692728.RA7E1erHTTKgsPH1Hzh5I3JB3TUXLSd0kk68oL9aTqr0Y130_assertion description "[Mutations in vascular endothelial growth factor (VEGF) receptor-3 (VEGFR3 or FLT4) cause Milroy disease, an autosomal dominant condition that presents with congenital lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692728.RA7E1erHTTKgsPH1Hzh5I3JB3TUXLSd0kk68oL9aTqr0Y130_provenance.
- NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_assertion description "[Mutations in vascular endothelial growth factor (VEGF) receptor-3 (VEGFR3 or FLT4) cause Milroy disease, an autosomal dominant condition that presents with congenital lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- assertion description "[Mutations in vascular endothelial growth factor (VEGF) receptor-3 (VEGFR3 or FLT4) cause Milroy disease, an autosomal dominant condition that presents with congenital lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion description "[Mutations in vascular endothelial growth factor (VEGF) receptor-3 (VEGFR3 or FLT4) cause Milroy disease, an autosomal dominant condition that presents with congenital lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_provenance.