Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_assertion description "[The novel findings included a set of genes (DCDC2, DYX1C1, KIAA0319) related to a neurological disease dyslexia suggesting their potential involvement in ciliary functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_assertion evidence source_evidence_literature NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_assertion SIO_000772 22558177 NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_assertion wasDerivedFrom befree-20140225 NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_assertion wasGeneratedBy ECO_0000203 NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP880790.RA8kRMb1CEngj0hUvfV3OOwVTd5WxTNEg9d7H-s8kepx8130_provenance.