Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_assertion description "[Genetically proven tumor predisposition syndromes (n = 14) frequently observed were syndromes associated with alterations of the chromosome WT1 region such as WAGR (n = 6) and Denys-Drash syndromes (n = 3), syndromes associated with alterations of the WT2 region (Beckwith-Wiedeman syndrome, n = 3), and Fanconi anemia (n = 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_assertion evidence source_evidence_literature NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_assertion SIO_000772 23970395 NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_assertion wasDerivedFrom befree-20150227 NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_assertion wasGeneratedBy ECO_0000203 NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP778587.RATLwUjC5oKO0M03h7jRZmkan6yeDRaa0zEXQImpP8o4g130_provenance.