Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion> ?p ?o ?g. }
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- NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion type Assertion NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_head.
- NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion wasGeneratedBy ECO_0000218 NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_provenance.
- NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion wasDerivedFrom uniprot-2016 NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_provenance.
- NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion SIO_000772 10856194 NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_provenance.
- NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion evidence source_evidence_curated NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_provenance.
- NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_assertion description "[Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867.RACgeunoWTPrS7UniCAAxb_a2dFCfZq05A8NXHVSHwtwg130_provenance.