Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_assertion description "[Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_assertion evidence source_evidence_literature NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_assertion SIO_000772 22271902 NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_assertion wasDerivedFrom befree-2016 NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_assertion wasGeneratedBy ECO_0000203 NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.
- befree-2016 importedOn "2016-02-19" NP955600.RALvQZ-hk8cbYoBMtDumGyeu2whOFCVe_kXdrTmvR1lOw130_provenance.