Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_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." NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_assertion evidence source_evidence_literature NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_assertion SIO_000772 12429635 NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_assertion wasDerivedFrom befree-20150227 NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_assertion wasGeneratedBy ECO_0000203 NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP703164.RAfMwVvkZrFblp7Ua2YiraglXSYLriWcGlemfwfor8V0Q130_provenance.