Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_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." NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_assertion evidence source_evidence_literature NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_assertion SIO_000772 22271902 NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_assertion wasDerivedFrom befree-20140225 NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_assertion wasGeneratedBy ECO_0000203 NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP635818.RAaPD1w3iSmj-9QNgkkTMPr1JEIM6cCFCAj08SbWoW4SM130_provenance.