Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_assertion wasGeneratedBy ECO_0000203 NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_assertion wasDerivedFrom befree-2016 NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_assertion SIO_000772 24413734 NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_assertion evidence source_evidence_literature NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.
- NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_assertion description "[These analyses identified highly recurrent epigenetic factor mutations in TET2, DNMT3A and IDH2 as well as a new highly prevalent RHOA mutation encoding a p.Gly17Val alteration present in 22 of 35 (67%) angioimmunoblastic T cell lymphoma (AITL) samples and in 8 of 44 (18%) PTCL, not otherwise specified (PTCL-NOS) samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1144140.RAwgK-qbj-LrAQEyzX4oJXMVMFZu0YO9p1FHlSjMXiD3I130_provenance.