Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_assertion description "[In contrast, chromosome aberrations were seen in 79% of early MDS samples and 90% of RAEB/AML samples, and were not as widely distributed over the genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_assertion evidence source_evidence_literature NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_assertion SIO_000772 18832655 NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_assertion wasDerivedFrom befree-20150227 NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_assertion wasGeneratedBy ECO_0000203 NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605872.RAGhssLPzoG_tUk6MS0W87fO72Hd-eYvPROOYxncTnavo130_provenance.