Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_assertion description "[CTNNB1 mutation was only found in one OC case, whereas three of six (50%) ameloblastoma cases and two out of eight (25%) OC cases had APC mutations within the mutational cluster region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_assertion evidence source_evidence_literature NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_assertion SIO_000772 18486530 NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_assertion wasDerivedFrom befree-20150227 NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_assertion wasGeneratedBy ECO_0000203 NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP336456.RA9KbHupmMXhn7MKuZVY8I-ZWZY2s6fooNFxyNwOLMbaM130_provenance.