Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion> ?p ?o ?g. }
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- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion type Assertion NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_head.
- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_provenance.
- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion evidence source_evidence_literature NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_provenance.
- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion SIO_000772 12676894 NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_provenance.
- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion wasDerivedFrom befree-20140225 NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_provenance.
- NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_assertion wasGeneratedBy ECO_0000203 NP676243.RADDiOaA_e_aWzYWSQzU69sy_rj_w8X1YykFJcJ4QWfTY130_provenance.