Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion> ?p ?o ?g. }
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- NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion type Assertion NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_head.
- NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion wasGeneratedBy ECO_0000203 NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_provenance.
- NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion wasDerivedFrom befree-2016 NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_provenance.
- NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion SIO_000772 18794123 NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_provenance.
- NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion evidence source_evidence_literature NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_provenance.
- NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_assertion description "[Activating mutations within fibroblast growth factor receptor 3 (FGFR3), a receptor tyrosine kinase, are responsible for human skeletal dysplasias including achondroplasia and the neonatal lethal syndromes, Thanatophoric Dysplasia (TD) type I and II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693191.RAAShCcdMv6qm1LuMqGyQXzi9G7HzoyNHRxAyzAgGkEoM130_provenance.