Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_assertion description "[These findings confirm that germline GATA2 mutations predispose to familial myelodysplastic syndrome/acute myeloid leukemia, and that monosomy 7 and ASXL1 mutations may be recurrent secondary genetic abnormalities triggering overt malignancy in these families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_assertion evidence source_evidence_literature NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_assertion SIO_000772 22271902 NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_assertion wasDerivedFrom befree-2016 NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_assertion wasGeneratedBy ECO_0000203 NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.
- befree-2016 importedOn "2016-02-19" NP955591.RAjybvMgYPVzoY-B82b2jDWE4VdouEDOOGZjf6gxzZSkE130_provenance.