Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_assertion description "[Since c.7271T>G is only one of many rare ATM variants predicted to have deleterious consequences on protein function, an effective means of identifying and grouping these variants is essential to assess the contribution of ATM variants to individual risk and to the incidence of breast cancer in the population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_assertion evidence source_evidence_literature NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_assertion SIO_000772 16958054 NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_assertion wasDerivedFrom gad-20130706 NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_assertion wasGeneratedBy ECO_0000203 NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP59602.RAmYWJatEtPSaOgH3RqHiCE-RBpnoigxNEgKnNYtgW3Hg130_provenance.