Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_assertion description "[This view is supported by the significant excess of unrelated clones observed in t-MDS following multiple myeloma (4 in 13 cases) compared with other diseases (9 in 167 cases; P = 0.02), and by results from a case with a balanced translocation that is highly characteristic of non-Hodgkin's lymphoma in one clone and a t-MDS-associated deletion of the long arm of chromosome 5 in another.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_assertion evidence source_evidence_literature NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_assertion SIO_000772 9824207 NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_assertion wasDerivedFrom befree-2016 NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_assertion wasGeneratedBy ECO_0000203 NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1409322.RALyi5HYxFRWfSCKHZyHRKrNGeYhFDzE9F4wCnaIC9UZo130_provenance.