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- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion type Assertion NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_head.
- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion description "[Mutations in SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_provenance.
- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion evidence source_evidence_literature NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_provenance.
- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion SIO_000772 17273969 NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_provenance.
- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion wasDerivedFrom lhgdn-20090331 NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_provenance.
- NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_assertion wasGeneratedBy ECO_0000203 NP222520.RA97XSySL4xjSh1NyY-SLcO6BlwTHYOHQ9evdQ22YYlEQ130_provenance.