Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion> ?p ?o ?g. }
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- NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion type Assertion NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_head.
- NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion description "[Rare individuals with PWS who carry atypical microdeletions on chromosome 15q have narrowed the critical region for this disorder to a 108 kb region that includes the SNORD116 snoRNA cluster and the Imprinted in Prader-Willi (IPW) non-coding RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_provenance.
- NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion evidence source_evidence_literature NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_provenance.
- NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion SIO_000772 24363065 NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_provenance.
- NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion wasDerivedFrom befree-20150227 NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_provenance.
- NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_assertion wasGeneratedBy ECO_0000203 NP673739.RAXTVdjsWmGeFyTLSlAqZxcXhEzGrnbBl3g33FOUpM3bM130_provenance.