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- source_evidence_literature type ECO_0000212 NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_assertion description "[Further aims were to compare karyotypic features of t-AML/t-MDS with de novo AML/MDS, in our material as well as in 5098 unselected, cyto- genetically abnormal, published cases, and to analyze associations between type of prior therapy and karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_assertion evidence source_evidence_literature NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_assertion SIO_000772 12454741 NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_assertion wasDerivedFrom befree-2016 NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_assertion wasGeneratedBy ECO_0000203 NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.
- befree-2016 importedOn "2016-02-19" NP375865.RAb1A3whYRbw2KYIMhrCUlVVU7AFI5ibEGUGfwyx26pXs130_provenance.