Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_assertion description "[Closely positioned somatic SETBP1 mutations encoding changes in Asp868, Ser869, Gly870, Ile871 and Asp880, which match germline mutations in Schinzel-Giedion syndrome (SGS), were detected in 17% of secondary acute myeloid leukemias (sAML) and 15% of chronic myelomonocytic leukemia (CMML) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_assertion evidence source_evidence_literature NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_assertion SIO_000772 23832012 NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_assertion wasDerivedFrom befree-20150227 NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_assertion wasGeneratedBy ECO_0000203 NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP881235.RA6Ps5jB5Ldf98cY_R7xkPcVImLH5v7D37WhKBSnZKu2E130_provenance.