Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_assertion description "[Class I and Class II mutations are significantly associated, indicating their cooperation in leukemogenesis The chromosome aberrations and gene mutations detected in the therapy-related and in the de novo subsets of MDS and AML are identical, although the frequencies with which they are observed may differ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_assertion evidence source_evidence_literature NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_assertion SIO_000772 18024656 NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_assertion wasDerivedFrom befree-2016 NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_assertion wasGeneratedBy ECO_0000203 NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.
- befree-2016 importedOn "2016-02-19" NP641129.RA1VnKIg1aMIkIuT1E9QXl-P5KCzv4o-rjBL1Z4_HSoSM130_provenance.