Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- befree-2016 importedOn "2016-02-19" NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_assertion wasGeneratedBy ECO_0000203 NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_assertion wasDerivedFrom befree-2016 NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_assertion SIO_000772 19246647 NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_assertion evidence source_evidence_literature NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.
- NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_assertion description "[The frequent presence of IDH1 mutations in secondary glioblastomas and their near-complete absence in primary glioblastomas reinforce the concept that despite their histological similarities, these subtypes are genetically and clinically distinct entities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722843.RA4aAdUj4yPpn1ZLOak5zfEZiq2p7CZfgEVdt8b4bL6c0130_provenance.