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- source_evidence_literature type ECO_0000212 NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_assertion description "[It is suggested that a similar enquiry into the mechanisms of chromosomal deletions in P-MDS is required in order to delineate the role of these abnormalities in the clonal evolution of this group of diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_assertion evidence source_evidence_literature NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_assertion SIO_000772 1732667 NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_assertion wasDerivedFrom befree-20150227 NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_assertion wasGeneratedBy ECO_0000203 NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781613.RApb6OYfQAi8mrIr9Nk9Na_Xc7hP0jXbTwsv7Z5-ASKFU130_provenance.