Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_assertion description "[A high incidence of somatically acquired point mutations in the AML1/RUNX1 gene has been reported in poorly differentiated acute myeloid leukemia (AML, M0) and in radiation-associated and therapy-related myelodysplastic syndrome (MDS) or AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_assertion evidence source_evidence_literature NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_assertion SIO_000772 14615365 NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_assertion wasDerivedFrom befree-20150227 NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_assertion wasGeneratedBy ECO_0000203 NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285366.RAMzb8HvPv4uuMUpFrKIieF776Uytl0Oz3IwlazX-ozUw130_provenance.