Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion> ?p ?o ?g. }
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- NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion type Assertion NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_head.
- 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.
- NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion evidence source_evidence_literature NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_provenance.
- NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion SIO_000772 23410910 NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_provenance.
- NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion wasDerivedFrom befree-2016 NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_provenance.
- NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_assertion wasGeneratedBy ECO_0000203 NP1053176.RAjyL14iXucaBOr9MR3zwE0NFNGYmCfrC7vg2WoVMIOZQ130_provenance.