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- source_evidence_literature type ECO_0000212 NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_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." NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_assertion evidence source_evidence_literature NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_assertion SIO_000772 18486530 NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_assertion wasDerivedFrom befree-20140225 NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_assertion wasGeneratedBy ECO_0000203 NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP349445.RAXkpB1YRs5jtSdUd-uRk2YBNYktOBdzUEVwtWOIf4EVo130_provenance.