Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_assertion description "[Notably, we identified the same FGFR1 mutations in a subset of H3F3A-mutated pediatric glioblastoma with additional alterations in the NF1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_assertion evidence source_evidence_literature NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_assertion SIO_000772 23817572 NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_assertion wasDerivedFrom befree-20150227 NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_assertion wasGeneratedBy ECO_0000203 NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443070.RAU6PnlPNqD12H47YrBGcZ2eimAsdRkxMk0l9zygBg1vU130_provenance.