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- NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_assertion type Assertion NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_head.
- NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_assertion wasGeneratedBy ECO_0000203 NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_provenance.
- NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_assertion wasDerivedFrom befree-20150227 NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_provenance.
- NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_assertion SIO_000772 12655498 NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_provenance.
- NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_assertion evidence source_evidence_literature NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_provenance.
- NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_assertion description "[A girl with a de novo interstitial deletion of the short arm of chromosome 1 (46,XX,del (1)(p22p32) is described with moderate developmental delay and minor phenotypic abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836358.RABVn9cOxqWcG6j0tOavKcZzdKWl7j3FN8vVVwwLilB9c130_provenance.