Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_assertion description "[Autosomal recessive ataxia with peripheral neuropathy and elevated AFP: novel mutations in SETX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_assertion evidence source_evidence_literature NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_assertion SIO_000772 16717225 NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_assertion wasDerivedFrom befree-20140225 NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_assertion wasGeneratedBy ECO_0000203 NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP410520.RAPeUAs4WeeOmMCeZoq1hrUYHORB4rAT53pvxHm-yvLz8130_provenance.