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- NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_assertion type Assertion NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_head.
- NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_assertion description "[The patient was found to carry a de novo PTPN11 mutation p.T2I as well as the maternally inherited NF1 mutation c.4661+1G>C. Her otherwise healthy mother and brother, who also had the NF1 mutation, showed few caf�-au-lait spots as the only sign of neurofibromatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_provenance.
- NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_assertion evidence source_evidence_literature NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_provenance.
- NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_assertion SIO_000772 19449407 NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_provenance.
- NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_assertion wasDerivedFrom befree-20150227 NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_provenance.
- NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_assertion wasGeneratedBy ECO_0000203 NP660372.RA7H_FEQlpImgC1h213Dt7bvmlWrPZ__sdgEla7N7gRho130_provenance.