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- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion type Assertion NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_head.
- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion wasGeneratedBy ECO_0000203 NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_provenance.
- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion wasDerivedFrom gad-20130706 NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_provenance.
- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion SIO_000772 17347258 NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_provenance.
- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion evidence source_evidence_literature NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_provenance.
- NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_assertion description "[The relationship between severe myoclonic epilepsy of infancy (SMEI or Dravet syndrome) and the related syndrome SMEI-borderland (SMEB) with mutations in the sodium channel alpha 1 subunit gene SCN1A is well established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66454.RAaJx9mXLPbvT7SqTiQ_k7LBNm1izO_x_5BPohtzrBEgk130_provenance.