Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_assertion description "[We used massively parallel sequencing to examine tumor samples collected from 87 patients with MDS before HSCT for coding mutations in 40 recurrently mutated MDS genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_assertion evidence source_evidence_literature NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_assertion SIO_000772 25092778 NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_assertion wasDerivedFrom befree-20150227 NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_assertion wasGeneratedBy ECO_0000203 NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914035.RATTkqAdsTD2LIg_ocwracAHO4cY2GI_ZDQ69c87rk6hI130_provenance.