Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_assertion description "[Missense FBXW7 mutations are prevalent in various tumors, including T�cell acute lymphoblastic leukemia (T-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_assertion evidence source_evidence_literature NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_assertion SIO_000772 23791182 NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_assertion wasDerivedFrom befree-20140225 NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_assertion wasGeneratedBy ECO_0000203 NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.
- befree-20140225 importedOn "2014-02-25" NP795529.RALIpS7YNspkJw-LwuqL_HQwHr0mwjz0OU4-Q67qzoxts130_provenance.