Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_assertion description "[Screening for SCA28, is warranted in patients who test negative for more common SCAs and present with a slowly progressive cerebellar ataxia accompanied by oculomotor signs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_assertion evidence source_evidence_literature NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_assertion SIO_000772 20725928 NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_assertion wasDerivedFrom befree-2016 NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_assertion wasGeneratedBy ECO_0000203 NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.
- befree-2016 importedOn "2016-02-19" NP834003.RAKj-TgtyN6FGOBKZ39bRIwAPHGexaROa8DJqG69fS7Tg130_provenance.