Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_assertion description "[Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_assertion evidence source_evidence_literature NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_assertion SIO_000772 16757412 NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_assertion wasDerivedFrom befree-20150227 NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_assertion wasGeneratedBy ECO_0000203 NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP387446.RAyK9arXMEdJ-B2ZjsFkFWNrlr38cU1r3SCziOS11n1jI130_provenance.