Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_assertion description "[MLL2, EP300, CREBBP, ASXL1) are also mutated in human developmental disorders thus pointing towards a remarkable and unexpected convergence between somatic and germline genetics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_assertion evidence source_evidence_literature NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_assertion SIO_000772 22287508 NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_assertion wasDerivedFrom befree-20150227 NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_assertion wasGeneratedBy ECO_0000203 NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978432.RACUoiJCIj2lxJiNSdWuw6IbvYbDW7VTjKDBZ9e8zy9xY130_provenance.