Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_assertion description "[Recessive mutations in CUBN or AMN cause Imerslund-Gr�sbeck Syndrome (IGS), while recessive mutations in GIF cause Intrinsic Factor Deficiency (IFD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_assertion evidence source_evidence_literature NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_assertion SIO_000772 22929189 NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_assertion wasDerivedFrom befree-20140225 NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_assertion wasGeneratedBy ECO_0000203 NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP921539.RAJlfvG28MfhGM0ZjyGvhXeWgOFP_qPrbGk0lM8LuTa7I130_provenance.