Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_assertion description "[Deletions and/or mutations of INI1 were detected in 75 patients, including 42 children with atypical teratoid/rhabdoid tumors of the brain or spinal cord and 6 children with a brain and a renal or soft-tissue tumor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_assertion evidence source_evidence_literature NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_assertion SIO_000772 12429635 NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_assertion wasDerivedFrom befree-20140225 NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_assertion wasGeneratedBy ECO_0000203 NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP802697.RAUklxFsGI0akjaieMjOZgK0bIPRAbJbzERED3uA3SqeA130_provenance.