Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_assertion description "[Further investigation revealed low levels of the glycoproteins AT III and clotting factor XI, leading to a diagnosis of congenital disorder of glycosylation (CDG) type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_assertion evidence source_evidence_literature NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_assertion SIO_000772 19067230 NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_assertion wasDerivedFrom befree-20140225 NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_assertion wasGeneratedBy ECO_0000203 NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP809066.RAtlPfEUthCfLRNDk8kIdpmHp2KXNswg3v_klDJovSlnY130_provenance.