Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_assertion description "[We report somatic heterozygous mutations in IDH1 (c.394C>T encoding an R132C substitution and c.395G>A encoding an R132H substitution) or IDH2 (c.516G>C encoding R172S) in 87% of enchondromas (benign cartilage tumors) and in 70% of spindle cell hemangiomas (benign vascular lesions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_assertion evidence source_evidence_literature NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_assertion SIO_000772 22057234 NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_assertion wasDerivedFrom befree-20150227 NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_assertion wasGeneratedBy ECO_0000203 NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475469.RAXvlYwRmduie0Z4V5o6EoVmtOVusP6gLF5l7aZ9siC4w130_provenance.