Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_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." NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_assertion evidence source_evidence_literature NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_assertion SIO_000772 17912431 NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_assertion wasDerivedFrom befree-20150227 NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_assertion wasGeneratedBy ECO_0000203 NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP300973.RALqQ0RpRoPnIl5WSCb56dn3TxNTFDeVUICIw8fjW-sSY130_provenance.