Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- befree-2016 importedOn "2016-02-19" NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_assertion wasGeneratedBy ECO_0000203 NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_assertion wasDerivedFrom befree-2016 NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_assertion SIO_000772 12874780 NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_assertion evidence source_evidence_literature NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.
- NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_assertion description "[AML1/RUNX1 mutations are infrequent, but related to AML-M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402811.RAGrw0qcYqEe2Vq_1-cTZPd79LSeZUySPG0MymxxRKGl0130_provenance.