Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_assertion description "[Spontaneous remission in 2 children with myelofibrosis, one with megakaryocytic acute myeloblastic leukemia and t(1;22) (with recurrence later) and one with Down syndrome and GATA1 mutation (permanent), are described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_assertion evidence source_evidence_literature NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_assertion SIO_000772 22627572 NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_assertion wasDerivedFrom befree-20150227 NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_assertion wasGeneratedBy ECO_0000203 NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP418781.RALLTBhA-GP3ZO1HuKMTxCMpHoFNFwQwRMv44r50ggWsk130_provenance.