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- source_evidence_literature type ECO_0000212 NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_assertion description "[These results suggested that mutation of the p16/CDKN2 gene was a common factor in the development of human MMMs and ACCs, while this gene may be correlated with development and/or progression of a subtype and play a role in the oncogenesis of these cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_assertion evidence source_evidence_literature NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_assertion SIO_000772 17912431 NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_assertion wasDerivedFrom befree-2016 NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_assertion wasGeneratedBy ECO_0000203 NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.
- befree-2016 importedOn "2016-02-19" NP633239.RAmQsTUyoL9tUknTjTHlcXvRr10uFo2ck7AM-XcqOHESk130_provenance.