Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_assertion description "[A BRAF p.Thr599dup or p.V600E mutation was identified by Sanger sequencing in one and five gliomas, respectively, and a somatic TP53 mutation was identified in a fibrillary astrocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_assertion evidence source_evidence_literature NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_assertion SIO_000772 24767714 NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_assertion wasDerivedFrom befree-20150227 NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_assertion wasGeneratedBy ECO_0000203 NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP271863.RAvSZIIAD4oPyrFYYakh2OtXlA5ueHJVmCTRQiYSuSHUo130_provenance.