Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_assertion description "[Furthermore, we found the methylation of p16 gene in three of seven patients lacking homozygous deletions, suggesting higher frequency of p16 inactivation than previous reports in T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_assertion evidence source_evidence_literature NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_assertion SIO_000772 10071127 NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_assertion wasDerivedFrom befree-20140225 NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_assertion wasGeneratedBy ECO_0000203 NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP351843.RAPEAPxkoFI7Rz5OqZsSruOvq6ZUoo0g57uUiEC0bEZdY130_provenance.