Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_assertion description "[Ataxia with vitamin E deficiency (AVED), or familial isolated vitamin E deficiency, is a rare autosomal recessive neurodegenerative disease characterized clinically by symptoms with often striking resemblance to those of Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_assertion evidence source_evidence_literature NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_assertion SIO_000772 9463307 NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_assertion wasDerivedFrom befree-2016 NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_assertion wasGeneratedBy ECO_0000203 NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1388575.RAKj5ho5C_5Jdcbn4Cx7Mmn3gHJEy8c_cCU3E1grqDmhI130_provenance.