Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_assertion description "[The ETV6-RUNX1 fusion is the molecular consequence of the t(12;21)(p13;q22) seen in approximately 25% of children with acute lymphoblastic leukemia (ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_assertion evidence source_evidence_literature NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_assertion SIO_000772 18767146 NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_assertion wasDerivedFrom befree-20140225 NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_assertion wasGeneratedBy ECO_0000203 NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP264930.RAv_ZxYjrojDRCNXLNKvawLNDEmx6DJjB812t3ssYyfzI130_provenance.