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- source_evidence_literature type ECO_0000212 NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_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." NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_assertion evidence source_evidence_literature NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_assertion SIO_000772 21889209 NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_assertion wasDerivedFrom befree-2016 NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_assertion wasGeneratedBy ECO_0000203 NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.
- befree-2016 importedOn "2016-02-19" NP921180.RA6xLx5cPCQSanhZNs-4oFVhJh3eO_WWpZT4vUJrjnY7I130_provenance.