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- source_evidence_literature type ECO_0000212 NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_assertion description "[Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_assertion evidence source_evidence_literature NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_assertion SIO_000772 25645639 NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_assertion wasDerivedFrom befree-2016 NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_assertion wasGeneratedBy ECO_0000203 NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260435.RANZ9cHI6dV9_drhvykFqoikkhfuAHeOv7SEeMAhL-LoM130_provenance.