Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_assertion description "[IDH1 and IDH2 mutations were detected in 72% of lower grade diffuse gliomas and in 17% of glioblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_assertion evidence source_evidence_literature NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_assertion SIO_000772 20431032 NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_assertion wasDerivedFrom befree-2016 NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_assertion wasGeneratedBy ECO_0000203 NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.
- befree-2016 importedOn "2016-02-19" NP809330.RAzzVel5fXyb7Foxl3lN4j43SPFVX212_5awo-oG07-p0130_provenance.