Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_assertion description "[To identify acquired somatic mutations associated with myeloid transformation in patients with GATA2 mutations, we sequenced the region of the ASXL1 gene previously associated with transformation from myelodysplasia to myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_assertion evidence source_evidence_literature NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_assertion SIO_000772 24077845 NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_assertion wasDerivedFrom befree-20150227 NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_assertion wasGeneratedBy ECO_0000203 NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978535.RA-TSH0gDUYzPF4gx49DR4JKO1NA3_fgoV55lbZTS9w0Y130_provenance.