Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- befree-2016 importedOn "2016-02-19" NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_assertion wasGeneratedBy ECO_0000203 NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_assertion wasDerivedFrom befree-2016 NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_assertion SIO_000772 21169275 NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_assertion evidence source_evidence_literature NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.
- NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_assertion description "[The results show that promoter methylation of p14, p15, p16, p21, p27, p57 and p73 was far more common in ESCC samples with CIMP+ than those with CIMP-.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860148.RAzqbZ2I_TAY4Pl3NnhYVqMpDWz6-XF7wfbLz-XNHgxnA130_provenance.