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- source_evidence_literature type ECO_0000212 NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_assertion description "[Mutation of the RAD51C gene in a Fanconi anemia-like disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_assertion evidence source_evidence_literature NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_assertion SIO_000772 20400963 NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_assertion wasDerivedFrom befree-2016 NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_assertion wasGeneratedBy ECO_0000203 NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.
- befree-2016 importedOn "2016-02-19" NP806788.RAnGCheJlXZlkGs_Kd3XjIFCydFEz6uTmmP9d69uFP1Nw130_provenance.