Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_assertion description "[We identified recurrent somatic mutations in ACVR1 exclusively in DIPGs (32%), in addition to previously reported frequent somatic mutations in histone H3 genes, TP53 and ATRX, in both DIPGs and NBS-HGGs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_assertion evidence source_evidence_curated NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_assertion SIO_000772 24705251 NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_assertion wasDerivedFrom ctd_human-20150221 NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_assertion wasGeneratedBy ECO_0000218 NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP7828.RAoVupX8cYVZHJ6b0Jlfv11hU9RKynW_-LJa2LBqQmwes130_provenance.