Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion description "[Indeed, the de novo methyltransferase 3B (DNMT3B) has been recently found to be mutated in several types of cancer and in the immunodeficiency, centromeric region instability and facial anomalies syndrome (ICF), in which these mutations could be related to the loss of global DNA methylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion evidence source_evidence_literature NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion SIO_000772 23474979 NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion wasDerivedFrom befree-20150227 NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion wasGeneratedBy ECO_0000203 NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance.