Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_assertion wasGeneratedBy ECO_0000203 NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_assertion wasDerivedFrom befree-20150227 NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_assertion SIO_000772 22445362 NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_assertion evidence source_evidence_literature NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.
- NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_assertion description "[IDH1 R132H mutation has been described as a common molecular signature of grade II and III diffuse gliomas and secondary glioblastoma; however, AG, which exhibits some features of diffuse glioma, has not been evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475139.RACNIqJkq1dOgR3yyGjr_liiZ2P8S6Cv1cjYrE8iEZ9EU130_provenance.