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- source_evidence_literature type ECO_0000212 NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_assertion description "[MEFV E148Q polymorphism is associated with Henoch-SchAPnlein purpura in Chinese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_assertion evidence source_evidence_literature NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_assertion SIO_000772 20602240 NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_assertion wasDerivedFrom gad-20150221 NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_assertion wasGeneratedBy ECO_0000203 NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP93182.RArT7q5hxu1sou5_ECS3d8_uxyZQ6wfFjqyFMyafjTCSo130_provenance.