Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_assertion description "[Deletions at chromosome 12p12-13 are observed in 26-47% of childhood pre-B acute lymphoblastic leukaemia (ALL) cases, suggesting the presence of a tumour suppressor gene (TSG).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_assertion evidence source_evidence_literature NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_assertion SIO_000772 17069581 NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_assertion wasDerivedFrom befree-2016 NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_assertion wasGeneratedBy ECO_0000203 NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.
- befree-2016 importedOn "2016-02-19" NP576502.RAIfmdx43n2CkTygpMwZ3BmwHA-uBXdifzLI5cOkbmC00130_provenance.