Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_assertion wasGeneratedBy ECO_0000203 NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_assertion wasDerivedFrom befree-20150227 NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_assertion SIO_000772 24081561 NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_assertion evidence source_evidence_literature NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.
- NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_assertion description "[Genetic risk scores for migraine and for MDD were used to predict pure and comorbid forms of migraine and MDD in an independent Dutch target sample (NTR-NESDA, N = 2,966), which included 1,476 MDD cases and 1,058 migraine cases (723 of these individuals had both disorders concurrently).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600798.RAALYkrb-6l186NXpkgYggbwi3LRNWU1L9FLT2_OvR0NM130_provenance.