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- source_evidence_literature type ECO_0000212 NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_assertion description "[The rs10994336 ANK3 and rs1006737 CACNA1C genetic variants have recently been identified as the most consistent, genome-wide significant risk factors for bipolar disorder, while the CACNA1C variant has also been associated with schizophrenia and major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_assertion evidence source_evidence_literature NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_assertion SIO_000772 21676128 NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_assertion wasDerivedFrom befree-20150227 NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_assertion wasGeneratedBy ECO_0000203 NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP238808.RAQUglE_x3vqn097OYXWsbFx-lluUO46k--h61GJ9SpuQ130_provenance.