Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion> ?p ?o ?g. }
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- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion type Assertion NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_head.
- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion description "[Mutations in cohesin complex members SMC3 and 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." NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_provenance.
- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion evidence source_evidence_literature NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_provenance.
- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion SIO_000772 17273969 NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_provenance.
- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion wasDerivedFrom befree-20140225 NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_provenance.
- NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_assertion wasGeneratedBy ECO_0000203 NP191449.RADd_rFiBrxKzlGeSfV0HqxwnPG2z5s3ZL9klVQKXQBXQ130_provenance.