Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_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." NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_assertion evidence source_evidence_literature NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_assertion SIO_000772 18587431 NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_assertion wasDerivedFrom befree-2016 NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_assertion wasGeneratedBy ECO_0000203 NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.
- befree-2016 importedOn "2016-02-19" NP679255.RAyPFCMSc1S9L3qEdQaeLSZcFjr_luOfXarkZ_l5WfALI130_provenance.