Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_assertion description "[Allogeneic SCT is important in myelodysplastic syndrome, the BCR-ABL-negative chronic myeloproliferative diseases (CMPDs) and in poor-risk AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_assertion evidence source_evidence_literature NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_assertion SIO_000772 18587431 NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_assertion wasDerivedFrom befree-20150227 NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_assertion wasGeneratedBy ECO_0000203 NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683766.RAvLwNfywfAWhz4t_U6HH7VkI1xZ5zoqtCtCntIrTVCSw130_provenance.