Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_assertion description "[The two dominant predisposing syndromes are familial adenomatous polyposis and Lynch syndrome, the first due to a mutant tumour-suppressor gene APC, and the second due to mutations in a number of genes responsible for mismatch repair in DNA at cell division.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_assertion evidence source_evidence_literature NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_assertion SIO_000772 11220653 NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_assertion wasDerivedFrom befree-20140225 NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_assertion wasGeneratedBy ECO_0000203 NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP336314.RAKkc6DiM2fiNEPcyT4ffM3uulUM6uTVIf67h8KQRwSeo130_provenance.