Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_assertion description "[Moreover, tissue-specific knock-in of Ptpn11(E76K/+) mutation in lineage-committed myeloid, T lymphoid, and B lymphoid progenitors also results in AML, T-ALL, and B-ALL, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_assertion evidence source_evidence_literature NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_assertion SIO_000772 21930766 NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_assertion wasDerivedFrom befree-2016 NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_assertion wasGeneratedBy ECO_0000203 NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP924798.RA5XClAOa2AZx6qikVkQHLZocEIqL8ACnOT90q4Aj9gfQ130_provenance.