Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion> ?p ?o ?g. }
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- NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion type Assertion NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_head.
- NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion description "[Most frequently, SRS is caused by altered gene expression on chromosome 11p15 due to hypomethylation of the telomeric imprinting center (ICR1) that is present in at least 40% of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_provenance.
- NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion evidence source_evidence_literature NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_provenance.
- NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion SIO_000772 21910219 NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_provenance.
- NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion wasDerivedFrom befree-2016 NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_provenance.
- NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_assertion wasGeneratedBy ECO_0000203 NP923116.RABLdfAtGBfUPaTJZ6G7nxOrJc9Gox2p-QJkNGM8iifVc130_provenance.