Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_assertion description "[The distribution of the treatment-related MDS cases was different than 'de novo' MDS with a high percentage of RAEB-T, and with the treatment related AMLs, there were a higher percentage of patients with FAB M6 (erythroleukemia), and no cases of FAB M3 (hypergranular promyelocytic).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_assertion evidence source_evidence_literature NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_assertion SIO_000772 3504435 NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_assertion wasDerivedFrom befree-20150227 NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_assertion wasGeneratedBy ECO_0000203 NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781404.RAEbqpYyXY0oZ27i6vJUQxSJNl2smufGQsdvXL9TeYwM4130_provenance.