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- NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_assertion type Assertion NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_head.
- NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_assertion description "[A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_provenance.
- NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_assertion evidence source_evidence_curated NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_provenance.
- NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_assertion SIO_000772 25714420 NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_provenance.
- NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_assertion wasDerivedFrom uniprot-2016 NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_provenance.
- NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_assertion wasGeneratedBy ECO_0000218 NP8150.RA_doBCM3Y3MjfucK8D8LsHOC4kRulIVbnByKUqo2moQ8130_provenance.