Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion> ?p ?o ?g. }
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- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion type Assertion NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_head.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_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." NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion evidence source_evidence_literature NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion SIO_000772 12676894 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion wasDerivedFrom befree-2016 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.
- NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_assertion wasGeneratedBy ECO_0000203 NP389818.RAQ9IHeXk-QTCfPz6u0z5qB7euIjc4vsaZaxb0aaCdzlU130_provenance.