Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_assertion description "[Normal karyotype was observed in 45.8 % of MDS (n = 44), 43.8 % of AML (n = 39) and 46.3 % of MPN (n = 82).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_assertion evidence source_evidence_literature NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_assertion SIO_000772 23389918 NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_assertion wasDerivedFrom befree-2016 NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_assertion wasGeneratedBy ECO_0000203 NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.
- befree-2016 importedOn "2016-02-19" NP1050967.RAfnKW6c2-0etwjTkWeV8EgvN9Po_SqGbBGOJs8lvL4ME130_provenance.