Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_assertion description "[The ataxia telangiectasia gene, ATM, is a candidate gene for this transformation because the complex karyotypes associated with BC of CML suggest that DNA double-strand break repair is defective and because the ABL pathway involves the interaction between the Abl and the Atm proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_assertion evidence source_evidence_literature NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_assertion SIO_000772 11516106 NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_assertion wasDerivedFrom befree-20140225 NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_assertion wasGeneratedBy ECO_0000203 NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650771.RAtb_cgmW9Fke-j9G46eeiDcCF8K5PpNQSWT-U1PE4w1Y130_provenance.