Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_assertion description "[The MLF1 and RARA genes are fused with NPM1 in myelodysplastic syndrome and acute myeloid leukemia (AML) with t(3;5) and acute promyelocytic leukemia with t(5;17), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_assertion evidence source_evidence_literature NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_assertion SIO_000772 16984370 NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_assertion wasDerivedFrom befree-20150227 NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_assertion wasGeneratedBy ECO_0000203 NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP665563.RA_EAai8-lRSWRqDqOjGnpXa4kncLVvGYBgBevvOh0r0Q130_provenance.