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- NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_assertion type Assertion NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_head.
- NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_assertion description "[Using microarray-based comparative genomic hybridization, 3 patients with epilepsy were revealed to have genomic copy number aberrations at 17p13.3: a partial LIS1 deletion in a patient with isolated lissencephaly and epilepsy, a triplication of LIS1 in a patient with symptomatic West syndrome, and a terminal deletion of 17p including YWHAE and CRK but not LIS1 in a patient with intractable epilepsy associated with distinctive facial features and growth retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_provenance.
- NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_assertion evidence source_evidence_literature NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_provenance.
- NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_assertion SIO_000772 20227246 NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_provenance.
- NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_assertion wasDerivedFrom befree-2016 NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_provenance.
- NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_assertion wasGeneratedBy ECO_0000203 NP799645.RAMFzISCYuCZ19nF6aY-S-clRV7RrqkNZ4DqFtJ5fYA6M130_provenance.