Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_assertion description "[Translocations and mutations in the core binding factor genes, RUNX1 or CBFB, are found in acute myeloid and lymphocytic leukemia, therapy-related myeloid leukemia, myelodysplastic syndrome, chronic myelomonocytic leukemia, and in familial platelet disorder with predisposition to acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_assertion evidence source_evidence_literature NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_assertion SIO_000772 22150309 NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_assertion wasDerivedFrom befree-2016 NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_assertion wasGeneratedBy ECO_0000203 NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.
- befree-2016 importedOn "2016-02-19" NP944763.RAzdEtnPF5LakJ4P3iHCSdRd45f2vUE4qTccoMQlGk2GA130_provenance.