Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_assertion description "[Trisomy 8 and an unbalanced t(5;17)(q11;p11) characterize two karyotypically independent clones in a case of idiopathic myelofibrosis evolving to acute nonlymphoid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_assertion evidence source_evidence_literature NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_assertion SIO_000772 2009512 NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_assertion wasDerivedFrom befree-20140225 NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_assertion wasGeneratedBy ECO_0000203 NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP605216.RADKidC5YDleNY8UZ_sdMLJz6sWpt4TNd_xTk3SXXHqBI130_provenance.