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- NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_assertion type Assertion NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_head.
- NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_assertion wasGeneratedBy ECO_0000203 NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_assertion wasDerivedFrom befree-20140225 NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_assertion SIO_000772 15691361 NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_assertion evidence source_evidence_literature NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_assertion description "[Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity in humans, is usually due to a de novo paternally derived chromosome 15q11-q13 deletion or maternal disomy 15 [(uniparental disomy (UPD)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.