Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP416996.RAbVXFMw67yh4eZSp47aMnRv7c20hUAPYreqG7urCeIQA130_provenance.