Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_assertion description "[MYH9-associated disorders (May-Hegglin anomaly, Epstein and Fechtner syndrome, and others) are inherited in an autosomal dominant manner and characterized by defects in different organs (including eyes, ears, kidneys and thrombocytes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_assertion evidence source_evidence_literature NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_assertion SIO_000772 23144074 NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_assertion wasDerivedFrom befree-2016 NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_assertion wasGeneratedBy ECO_0000203 NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1027658.RAnitSPVfJ6x0yzsPeKzDvl92mA0YewuJugSkGPB1-EVQ130_provenance.