Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_assertion description "[Our results suggest that in our population the NQO1 C609T polymorphism does not confer an increased risk of the investigated entities of childhood ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_assertion evidence source_evidence_literature NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_assertion SIO_000772 15590400 NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_assertion wasDerivedFrom gad-20150221 NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_assertion wasGeneratedBy ECO_0000203 NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP89430.RAwrpfGhCHb1yBTceamL2jAWqvh613myeDBlHjeYpEbQs130_provenance.