Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP180612.RAk6sS2OqOiLHmlD8lMVYDkrQ4l1lTn5mheh7IVIyN3-Q130_provenance.