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- source_evidence_literature type ECO_0000212 NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_assertion description "[In every individual with FDH, the mutation was associated with the Sac I+ polymorphism in the albumin gene, strongly suggesting a founder effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_assertion evidence source_evidence_literature NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_assertion SIO_000772 8048949 NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_assertion wasDerivedFrom befree-20150227 NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_assertion wasGeneratedBy ECO_0000203 NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP865519.RAKOup4OGq5b2j40EIhDG8ri1d_8xChDzwTROgq89NCDg130_provenance.