Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_assertion description "[Frequencies were in detail: acute myeloid leukemia (AML): 40 of 3,798, 1.1%; myelodysplastic syndromes (MDS): 6 of 3,375, 0.2%; myeloproliferative neoplasms (MPNs): 5 of 1,720, 0.3%; MDS/MPN: 0 of 210; and chronic myelomonocytic leukemia: 0 of 447.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_assertion evidence source_evidence_literature NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_assertion SIO_000772 22162288 NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_assertion wasDerivedFrom befree-20150227 NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_assertion wasGeneratedBy ECO_0000203 NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP953884.RAII2e3xtSRei_l8YnEEi8YgPzTxKgdNEnYKLYbiwL-TM130_provenance.