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- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion type Assertion NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_head.
- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion wasGeneratedBy ECO_0000203 NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_provenance.
- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion wasDerivedFrom befree-20140225 NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_provenance.
- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion SIO_000772 19191227 NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_provenance.
- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion evidence source_evidence_literature NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_provenance.
- NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_assertion description "[In addition, de novo LGI1 mutations are found in about 2% of sporadic cases with idiopathic partial epilepsy with auditory features, who are clinically similar to the majority of patients with ADLTE/ADPEAF but have no family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382333.RAOyZdhcgVfkBLg-N_uzvzR-wCCgxpCASyUZmmrdB2sh8130_provenance.