Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion> ?p ?o ?g. }
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- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion type Assertion NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_head.
- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion description "[Nine probands with a firm clinical diagnosis of PWS but who had neither a typical deletion in the PWS region nor UPD(15)mat were investigated for inactivating mutations in 11 genes located in the PWS region, including SNURF and SNRPN, which are associated with the imprinting centre.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_provenance.
- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion evidence source_evidence_literature NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_provenance.
- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion SIO_000772 17262171 NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_provenance.
- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion wasDerivedFrom befree-2016 NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_provenance.
- NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_assertion wasGeneratedBy ECO_0000203 NP591321.RASNGInruj75L3z4iHoM2OgTO39mCoY4hBFRnTKxtIDp8130_provenance.