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- NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_assertion type Assertion NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_head.
- NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_assertion description "[In this article, we report the cases of three children who (1) had manifested mildly different symptomatic neuropathy (twins, aged 4 years; and a boy, aged 9 years) associated with massive, symmetrical neurofibromas; (2) had few caf�-au-lait spots with irregular margins and pale brown pigmentation; (3) were presented with, at brain magnetic resonance imaging (MRI), bilateral, NF1-like high-signal abnormalities in the basal ganglia; (4) yielded missense NF1 gene mutations in exon 39; and (5) had unaffected parents with negative NF1 genetic testing as well as discuss 12 families and 20 sporadic and 5 additional cases that presented spinal neurofibromatosis within classical NF1 families (53 cases) that were reported in the literature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_provenance.
- NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_assertion evidence source_evidence_literature NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_provenance.
- NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_assertion SIO_000772 23780384 NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_provenance.
- NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_assertion wasDerivedFrom befree-2016 NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_provenance.
- NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_assertion wasGeneratedBy ECO_0000203 NP1087204.RAaBHbslSyxBMQ3dGh-wHaizPRaMu-gm-JcDstE9x6Mag130_provenance.