Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion> ?p ?o ?g. }
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- NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion type Assertion NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_head.
- NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion description "[Here, we report that 18 of 231 individuals with Noonan syndrome without known mutations (corresponding to 3% of all affected individuals) and two of six individuals with LEOPARD syndrome without PTPN11 mutations have missense mutations in RAF1, which encodes a serine-threonine kinase that activates MEK1 and MEK2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_provenance.
- NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion evidence source_evidence_literature NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_provenance.
- NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion SIO_000772 17603483 NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_provenance.
- NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion wasDerivedFrom befree-20140225 NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_provenance.
- NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_assertion wasGeneratedBy ECO_0000203 NP488803.RApCZD0XI4RWa0KQuDY44YW0EFC0hiRDaaLFv2fuuoIBY130_provenance.