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- source_evidence_literature type ECO_0000212 NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_assertion description "[Role of 657del5 NBN mutation and 7p12.2 (IKZF1), 9p21 (CDKN2A), 10q21.2 (ARID5B) and 14q11.2 (CEBPE) variation and risk of childhood ALL in the Polish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_assertion evidence source_evidence_literature NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_assertion SIO_000772 21889209 NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_assertion wasDerivedFrom befree-20150227 NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_assertion wasGeneratedBy ECO_0000203 NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP955057.RAj6xnisKV3gdNpF7ORMbKCBhe-TmMO5qF8gx1YZ2kZ-Y130_provenance.