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- source_evidence_literature type ECO_0000212 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion evidence source_evidence_literature NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion SIO_000772 15596616 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion wasDerivedFrom befree-20150227 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_assertion wasGeneratedBy ECO_0000203 NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP782590.RAXc5MJgoFeMFwgI2gHy7FlCpD5omdT6aiStFv-8XRoeQ130_provenance.