Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion> ?p ?o ?g. }
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- NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion type Assertion NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_head.
- NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion description "[Fluorescence in situ hybridization (FISH) using cosmid probes for SNRPN, D15S10, and GABRB3 for the Prader-Willi syndrome (PWS)/Angelman syndrome (AS) critical region were not present on the derived chromosome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion evidence source_evidence_literature NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion SIO_000772 9128934 NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion wasDerivedFrom befree-20150227 NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_assertion wasGeneratedBy ECO_0000203 NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.