Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion> ?p ?o ?g. }
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- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion type Assertion NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_head.
- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_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." NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_provenance.
- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion evidence source_evidence_literature NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_provenance.
- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion SIO_000772 17273969 NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_provenance.
- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion wasDerivedFrom lhgdn-20090331 NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_provenance.
- NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_assertion wasGeneratedBy ECO_0000203 NP153757.RAFKg55t0-kjmw9n_DveJFZPOi8FYkPbnBXWzkaHO5gvg130_provenance.