Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion> ?p ?o ?g. }
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- NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion type Assertion NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_head.
- NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion description "[A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_provenance.
- NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion evidence source_evidence_literature NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_provenance.
- NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion SIO_000772 17668384 NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_provenance.
- NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion wasDerivedFrom befree-20150227 NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_provenance.
- NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_assertion wasGeneratedBy ECO_0000203 NP835527.RAlFM_UlR9whJp0zO6QoVTS_twEYA3SsT5bFKZS2HT7JQ130_provenance.