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- NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_assertion type Assertion NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_head.
- NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_assertion wasGeneratedBy ECO_0000203 NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_provenance.
- NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_assertion wasDerivedFrom lhgdn-20090331 NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_provenance.
- NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_assertion SIO_000772 12887446 NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_provenance.
- NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_assertion evidence source_evidence_literature NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_provenance.
- NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_assertion description "[Evidence for S284L mutation of the CHRNA4 in a white family with autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151673.RALj0KTHgg-OXmKvV9OYO1IA84QTn-s3V7ioCASVNmPF8130_provenance.