Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_assertion description "[Through exomic sequencing of 32 intrahepatic cholangiocarcinomas, we discovered frequent inactivating mutations in multiple chromatin-remodeling genes (including BAP1, ARID1A and PBRM1), and mutation in one of these genes occurred in almost half of the carcinomas sequenced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_assertion evidence source_evidence_literature NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_assertion SIO_000772 24185509 NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_assertion wasDerivedFrom befree-20150227 NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_assertion wasGeneratedBy ECO_0000203 NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP917033.RA_0PVLJRqNS6lCfsPaV6P5hzUg5hatVCbQIliRxgnSRw130_provenance.