Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_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." NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_assertion evidence source_evidence_literature NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_assertion SIO_000772 25092778 NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_assertion wasDerivedFrom befree-20150227 NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_assertion wasGeneratedBy ECO_0000203 NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP605998.RA7-2pwOz6ZRl1izswD3JR_kcrcq7koSZrr-MNBDEowzQ130_provenance.