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- source_evidence_literature type ECO_0000212 NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_assertion description "[Whereas mutations in ADAMTS17 have recently been identified in autosomal recessive Weill-Marchesani-like syndrome in humans and dogs presenting with ophthalmologic, cardiac, and skeletal abnormalities, no disease associations have been described for CERS3 (ceramide synthase 3) and FLJ42289 so far.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_assertion evidence source_evidence_literature NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_assertion SIO_000772 23754960 NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_assertion wasDerivedFrom befree-20140225 NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_assertion wasGeneratedBy ECO_0000203 NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP782651.RAtAa1XSikx0AcoLg9ROhzQ6Ux-HlpC3_hS5Lhyk1Kd4A130_provenance.