Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion> ?p ?o ?g. }
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- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion type Assertion NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_head.
- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion wasGeneratedBy ECO_0000203 NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_provenance.
- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion wasDerivedFrom befree-20150227 NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_provenance.
- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion SIO_000772 19191227 NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_provenance.
- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_assertion evidence source_evidence_literature NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_provenance.
- NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_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." NP817531.RAjHz2SyXu-XFPC47JuvDcpwn1je3IiWITCfK4EuPbxUQ130_provenance.