Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_assertion description "[Cells from the patient were characterized by chromosomal instability; radiosensitivity; failure to form DNA damage-induced MRN foci; and impaired radiation-induced activation of and downstream signaling through the ATM protein, which is defective in the human genetic disorder ataxia-telangiectasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_assertion evidence source_evidence_literature NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_assertion SIO_000772 19409520 NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_assertion wasDerivedFrom befree-20140225 NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_assertion wasGeneratedBy ECO_0000203 NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP697197.RAaXoNG5SXIgYJf44F5-d87W8-eeQq9XLjfs1sN133TUo130_provenance.