Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_assertion description "[Renal function was normal except for 1 patient with a MLL2 mutation diagnosed in the first days of life and severe renal disease due to unilateral renal agenesia and controlateral severe hypoplasia that progressed to the terminal stage at age 2 years.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_assertion evidence source_evidence_literature NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_assertion SIO_000772 23535010 NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_assertion wasDerivedFrom befree-20150227 NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_assertion wasGeneratedBy ECO_0000203 NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP829922.RAGP1OmWfHI5ZZJtN0KI9PUaWA7nDW7bmJsGV8gJvRJcg130_provenance.