Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_assertion wasGeneratedBy ECO_0000203 NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_assertion wasDerivedFrom befree-20150227 NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_assertion SIO_000772 24272205 NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_assertion evidence source_evidence_literature NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.
- NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_assertion description "[Seven HG-IEN lesions shared an identical mutational profile with the EGC from the same patient; 13 mutations observed in APC, ATM, FGFR3, PIK3CA, RB1, STK11, and TP53 genes were shared by both HG-IEN and ECG lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648398.RAieWzGrF8YgwEk4TjGZuHuc96xjLHFn_lNm2EFU9hr9M130_provenance.