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- source_evidence_literature type ECO_0000212 NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_assertion description "[In a genome-wide association study we found highly significant associations between RLS and intronic variants in the homeobox gene MEIS1, the BTBD9 gene encoding a BTB(POZ) domain as well as variants in a third locus containing the genes encoding mitogen-activated protein kinase MAP2K5 and the transcription factor LBXCOR1 on chromosomes 2p, 6p and 15q, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_assertion evidence source_evidence_literature NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_assertion SIO_000772 17637780 NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_assertion wasDerivedFrom gad-20130706 NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_assertion wasGeneratedBy ECO_0000203 NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP77446.RAGiKg-rB9w-8J5ZcL8SGI1r_J4PaSIXoQ6NU5lSVAkE0130_provenance.