Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_assertion description "[GATA1 mutations in Down syndrome and its altered role in DS and myeloid leukemia may lead to an increased understanding of why children with DS are markedly predisposed to leukemia.(review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_assertion evidence source_evidence_literature NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_assertion SIO_000772 14512321 NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_assertion wasDerivedFrom lhgdn-20090331 NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_assertion wasGeneratedBy ECO_0000203 NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP131066.RACcvc3wlhUIIU0WA-m7EjgPIP4JJgiPxu-rsFqUs4aJM130_provenance.