Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_assertion description "[We therefore conclude that the presence of a homozygous p16 deletion may well be an important risk factor for both relapse and death in childhood ALL, and that its prognostic effect is not a consequence of confounding by other factors already known to influence outcome in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_assertion evidence source_evidence_literature NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_assertion SIO_000772 9166859 NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_assertion wasDerivedFrom befree-20140225 NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_assertion wasGeneratedBy ECO_0000203 NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.
- befree-20140225 importedOn "2014-02-25" NP488443.RAgjthQO69eKZmFEPZAoOVwbp4w2L6yMRXeb88in3U140130_provenance.